|
Pacira BioSciences, Inc. (PCRX): Business Model Canvas [Dec-2025 Updated] |
Fully Editable: Tailor To Your Needs In Excel Or Sheets
Professional Design: Trusted, Industry-Standard Templates
Investor-Approved Valuation Models
MAC/PC Compatible, Fully Unlocked
No Expertise Is Needed; Easy To Follow
Pacira BioSciences, Inc. (PCRX) Bundle
You're analyzing a specialty pharma firm balancing near-term sales against long-term innovation, and Pacira BioSciences, Inc. is a prime example of that tightrope walk. As we look at late 2025, the company is driving its 5x30 strategy, targeting total revenue guidance between $725 million and $735 million for the year, while still earmarking $95M to $105M for R&D investment into its next generation of non-opioid pain treatments. Honestly, figuring out how they structure their costs-like the high SG&A spend versus their $246.3 million cash position in Q3-is crucial to understanding the sustainability of their value proposition centered on EXPAREL and ZILRETTA. Scroll down to see the full nine-block Business Model Canvas that maps out exactly how Pacira BioSciences, Inc. generates revenue and defends its market position.
Pacira BioSciences, Inc. (PCRX) - Canvas Business Model: Key Partnerships
You're looking at how Pacira BioSciences, Inc. extends its reach and pipeline through external relationships, which is crucial for a company executing a transition like the '5x30' plan.
Johnson & Johnson MedTech for ZILRETTA co-promotion
In July 2025, Pacira BioSciences entered a strategic co-promotion agreement with Johnson & Johnson MedTech for ZILRETTA (triamcinolone acetonide extended-release injectable suspension). This alliance is designed to expand ZILRETTA's reach by utilizing Johnson & Johnson MedTech's early intervention sales force. The partnership targets broadening access across a significant portion of the estimated seven million annual knee injections administered in the U.S. for osteoarthritis (OA) knee pain.
Group Purchasing Organizations (GPOs) for market access
Market access through GPOs remains a focus for commercial products like EXPAREL. As of June 30, 2024, the company noted that its 3 GPOs collectively cover approximately ~2/3 of EXPAREL TAM (Total Addressable Market). The impact of these arrangements is visible in recent sales figures; for instance, EXPAREL net product sales in the second quarter of 2025 saw some discounting associated with the launch of a new GPO partnership.
GQ Bio Therapeutics (now fully acquired) for gene therapy platform
Pacira BioSciences completed the acquisition of the remaining 81 percent equity stake in GQ Bio Therapeutics GmbH in February 2025. The total cost was approximately $32 million, net of working capital adjustments. This transaction included $18 million paid at closing, with an additional $8 million committed over three years for key employee retention.
This acquisition was financially beneficial as it eliminated up to $64 million in potential future milestone payments, including a $4.5 million payment tied to the initiation of the Phase 2 clinical trial for PCRX-201. The core asset gained is GQ Bio's high-capacity adenovirus (HCAd) gene therapy vector platform.
Key financial details of the GQ Bio acquisition:
| Transaction Component | Amount (USD) |
| Total Acquisition Cost (Approximate) | $32 million |
| Cash Paid at Closing | $18 million |
| Future Employee Retention Commitment | $8 million (over three years) |
| Milestone Payments Eliminated (Maximum) | Up to $64 million |
Third-party licensees for bupivacaine liposome suspension
Pacira BioSciences generates revenue through licensing its bupivacaine liposome injectable suspension for veterinary use to third-party licensees. Sales figures show consistent, albeit small, revenue streams from this channel.
- Sales to third-party licensees in the first quarter of 2025 were $2.6 million, up from $2.5 million in Q1 2024.
- Sales to third-party licensees in the third quarter of 2025 reached $2.7 million, a notable increase from $1.6 million in Q3 2024.
- Total other revenue, which includes these royalties, was $11.1 million for the full year 2024.
Separately, in July 2025, Pacira BioSciences received a $28.3 million cash payment following a U.S. District Court judgment in Nevada, which declared that the Research and Development Foundation (RDF) must repay royalties previously paid under protest on EXPAREL sales, plus $5.2 million in statutory interest.
Academic institutions for Investigator-Initiated Trials (IITs)
Pacira BioSciences supports Investigator-Initiated Trials (IITs) conducted in the United States. These research studies are designed and sponsored by the principal investigator or institution, providing Pacira BioSciences with valued information on the safety, efficacy, pharmacology, and tolerability of its marketed products.
The company reviews applications for IIT support based on several criteria:
- Scientific merit and innovation.
- Clinical impact on patients.
- Compliance with Pacira policy and requirements.
Areas of therapeutic interest for IIT support include:
- Outcomes of opioid-free perioperative pathways.
- Long-term outcomes of enhanced recovery pathways (including functional and patient-reported outcomes 30+ days).
The Phase 2 ASCEND study for PCRX-201, while not an IIT, surpassed 50% enrollment in Part A during the second quarter of 2025, involving approximately 135 patients in total.
Pacira BioSciences, Inc. (PCRX) - Canvas Business Model: Key Activities
Commercialization and market expansion of EXPAREL
- - EXPAREL net product sales for the third quarter of 2025 were $139.9 million.
- - Third quarter 2025 EXPAREL volume growth was 9 percent year-over-year.
- - Total revenues for the third quarter of 2025 reached $179.5 million.
- - ZILRETTA net product sales for the third quarter of 2025 were $29.0 million.
- - Third quarter 2025 iovera° net product sales were $6.5 million.
- - Commercial coverage is estimated at approximately 60 million commercial lives.
- - Total covered population across commercial and government payers is nearly 90 million lives.
- - Over 90% of EXPAREL business now has contracted pricing through group purchasing organizations (GPOs) or individual agreements.
Research and development (R&D) for new pipeline assets like PCRX-201
- - Patient enrollment concluded in Part A of the Phase 2 ASCEND study for PCRX-201 in November 2025.
- - PCRX-201 demonstrated sustained improvements through three years (156 weeks) in a Phase 1 clinical trial.
- - Topline results from Part A of the Phase 2 study are expected near the end of 2026.
- - Full-year 2025 non-GAAP R&D expense guidance is projected to be $95-105 million.
- - Non-GAAP R&D expense for the third quarter of 2025 was $22.5 million.
Manufacturing and quality control of proprietary DepoFoam technology
| Metric | 2024 Level | Q3 2025 Actual | 2025 Guidance Range |
| Non-GAAP Gross Margin | 76% (2024 level) | 82% | 80-82% |
Managing intellectual property (IP) and patent defense (e.g., EXPAREL exclusivity to 2039)
- - Unlimited generic production of EXPAREL is licensed to begin no earlier than 2039.
- - Limited generic entry is permitted starting in early 2030, with volumes gradually increasing to a maximum in the high thirties by the final years.
- - A new patent for the manufacturing process has an expiration date of January 22, 2041.
- - The last-to-expire of Pacira\'s Orange Book-listed patents for EXPAREL is July 2, 2044.
Executing the 5x30 long-term growth plan
The 5x30 plan sets five objectives to achieve by 2030:
- - Patients: More than three million patients treated per year.
- - Product revenue: Double-digit compounded annual growth rate.
- - Profitability: Five percentage point gross margin improvement over 2024 levels.
- - Pipeline: Clinical pipeline expansion with five novel programs in development.
- - Partnerships: Establishing five partnerships including pipeline and commercial agreements.
Key financial metrics supporting the 5x30 execution as of late 2025:
| Financial Item | Reported/Guidance Amount |
| Full-Year 2025 Total Revenue Guidance | $725-735 million |
| Q3 2025 Adjusted EBITDA | $49.4 million |
| Cash, Cash Equivalents, and Investments (End of Q3 2025) | $246.3 million |
| Shares Repurchased in Q3 2025 | 2.0 million shares for a cost of $50.0 million |
Pacira BioSciences, Inc. (PCRX) - Canvas Business Model: Key Resources
You're looking at the core assets that power Pacira BioSciences, Inc. as of late 2025. These aren't just line items; they are the protected technologies and the financial muscle backing the company's strategy.
Intellectual Property and Regulatory Assets
- - EXPAREL and ZILRETTA patents and regulatory approvals: The intellectual property estate for EXPAREL remains a significant barrier to entry.
- - The last-to-expire Orange Book-listed patent for EXPAREL has a date of July 2, 2044.
- - In April 2025, Pacira BioSciences, Inc. settled patent litigations, establishing an exclusivity runway for EXPAREL extending to 2039 for unlimited generic entry, with a volume-limited license beginning sometime in early 2030.
- - In November 2025, the company filed patent infringement lawsuits against The WhiteOak Group and Qilu Pharmaceutical, which triggered a 30-month stay on FDA approval for their proposed generic versions.
- - The iovera° system received FDA 510k clearance in January 2025 for a new Smart Tip targeting chronic low back pain.
- - The indication for iovera° is to block and/or relieve pain for up to 90 days.
Proprietary Technology Platforms
Pacira BioSciences, Inc. relies on its established and newly acquired delivery platforms to create long-acting, locally administered treatments.
- - Proprietary drug delivery platforms (DepoFoam and HCAd vector): The DepoFoam technology is the proven delivery system for EXPAREL.
- - The novel high-capacity adenovirus (HCAd) vector platform was integrated via the acquisition of GQ Bio Therapeutics in February 2025.
- - The HCAd vector platform can carry up to 30,000 base pairs of DNA, allowing for gene therapy with multiple or larger genes.
Financial Strength and Commercial Infrastructure
The balance sheet provides the capital for ongoing defense of IP and investment in the pipeline. Here's the quick math on the cash position as of the end of Q3 2025.
| Financial Metric | Amount as of Q3 2025 |
| Cash, Cash Equivalents, and Available-for-Sale Investments | $246.3 million |
| iovera° Net Product Sales (Q3 2025) | $6.5 million |
| Non-GAAP Selling, General & Administrative (SG&A) Expenses (Q3 2025) | $81.7 million |
| Year-over-Year Growth in Non-GAAP SG&A (Q3 2025) | 26% |
The investment in the commercial engine is reflected in the SG&A spend, which includes the specialized US sales and clinical support team. This team supports the commercial products, including EXPAREL net sales of $139.9 million in Q3 2025.
The iovera° cryoanalgesia system technology is a commercial asset that generated net product sales of $6.5 million in the third quarter of 2025.
Finance: draft 13-week cash view by Friday.
Pacira BioSciences, Inc. (PCRX) - Canvas Business Model: Value Propositions
You're looking at the core reasons why surgeons and hospitals choose Pacira BioSciences, Inc.'s products over alternatives, especially when managing pain without relying on opioids. The value proposition centers on superior patient outcomes, cost-effectiveness through reduced hospital stays, and a pipeline focused on chronic pain.
The flagship offering, a long-acting, non-opioid pain management solution for post-surgery, continues to drive significant revenue. For instance, in the third quarter of 2025, net product sales for this product reached $139.9 million, reflecting a strong 9 percent year-over-year volume growth. This growth is key to the company's strategy, as it now has expanded access, with approximately 60 million commercial lives covered via a separate reimbursement mechanism, contributing to a total covered population of nearly 90 million lives across commercial and government payers. This product demonstrated in studies a potential for up to a 78 percent decrease in opioid consumption following a single injection.
For chronic conditions, the extended-release relief for osteoarthritis knee pain is another pillar. In the third quarter of 2025, net product sales for this treatment were $29.0 million. This product's performance, alongside the others, helped push Pacira BioSciences' third-quarter non-GAAP gross margin to 82%, up from 78% in the prior year's third quarter.
The value extends to procedural pain relief via cryoanalgesia, with third-quarter 2025 net product sales hitting $6.5 million. This portfolio strength underpins the company's financial health, as evidenced by the $49.4 million in Adjusted EBITDA reported for the third quarter of 2025, and the company raising its full-year 2025 non-GAAP gross margin guidance to 80% to 82%.
Here's a quick look at the recent product performance that defines these value propositions:
| Product | Value Proposition Focus | Q3 2025 Net Product Sales (Millions USD) | Year-over-Year Volume Growth (Q3 2025) |
| Long-acting, non-opioid pain management post-surgery | Opioid-sparing care, reduced consumption | $139.9 | 9 percent |
| Extended-release relief for osteoarthritis knee pain | Non-opioid treatment for chronic/joint pain | $29.0 | Not explicitly stated for volume, but sales grew from $28.4 million in Q3 2024 |
| Targeted, non-pharmacologic pain relief via cryoanalgesia | Non-opioid localized relief | $6.5 | Not explicitly stated for volume, but sales grew from $5.7 million in Q3 2024 |
The commitment to opioid-sparing care is further supported by regulatory and legislative tailwinds. The NOPAIN Act is now in effect, creating a reimbursement pathway for 18 million outpatient surgical procedures where EXPAREL can be used. This directly supports the value of reducing hospital stay and addiction risk by enabling non-opioid options in settings where they were previously harder to cover.
Looking to the future, the innovative gene therapy platform is being developed to address chronic pain at its cause. Pacira BioSciences, Inc. acquired the underlying technology, the high-capacity adenovirus (HCAd) vector platform, in February 2025. This platform is designed to carry up to 30,000 base pairs of DNA, which is significantly more than many AAV vectors, potentially allowing for more complex or multiple genes in a single therapy. The lead candidate, PCRX-201 for knee osteoarthritis, has already received Regenerative Medicine Advanced Therapy (RMAT) designation from the FDA, and as of the second quarter of 2025, the Phase 2 ASCEND study had surpassed 50% enrollment.
These platform advancements represent the long-term value proposition:
- - Long-acting, non-opioid pain management post-surgery (EXPAREL): $139.9 million in Q3 2025 net product sales.
- - Extended-release relief for osteoarthritis knee pain (ZILRETTA): $29.0 million in Q3 2025 net product sales.
- - Opioid-sparing care that reduces hospital stay and addiction risk: Reimbursement pathway now covers 18 million outpatient procedures via the NOPAIN Act.
- - Targeted, non-pharmacologic pain relief via cryoanalgesia (iovera°): $6.5 million in Q3 2025 net product sales.
- - Innovative gene therapy platform for chronic pain (HCAd platform): Vector capacity of up to 30,000 base pairs of DNA.
Pacira BioSciences, Inc. (PCRX) - Canvas Business Model: Customer Relationships
You're looking at how Pacira BioSciences, Inc. manages the people who use and influence their non-opioid pain therapies. This is all about the direct interaction and support structure they use to drive adoption of EXPAREL, ZILRETTA, and iovera°.
Dedicated, high-touch clinical education and support
Pacira BioSciences, Inc. has been actively reshaping its commercial structure to better serve customers. Following a sales force restructuring, the company reorganized into dedicated teams for EXPAREL, ZILRETTA, and iovera° as of mid-2025. As of December 31, 2024, the organization had 790 employees. The company is focused on communicating advances in market access to customers to encourage expanded utilization.
The support extends to specific product reimbursement mechanisms. For iovera°, the product-specific code C-9809 allows physicians to receive up to $256 for its use.
Direct relationship management with key hospital accounts and IDNs
Direct relationship management is being augmented through strategic alliances. Pacira BioSciences, Inc. entered a strategic collaboration with Johnson & Johnson MedTech in Q2 2025 to co-promote ZILRETTA, leveraging J&J's specialized early intervention sales force to reach existing and new customers. The company's 5x30 strategy includes a goal to establish five partnerships by 2030 to expand commercial reach. The company is focused on driving broad market adoption for EXPAREL.
| Metric | Value/Target | Date/Context |
| EXPAREL Volume Growth (Q1 2025 vs Q1 2024) | 7 percent | First Quarter 2025 |
| ZILRETTA/iovera° Performance Post-Restructuring | Flat to slightly declining | First Quarter 2025 |
| Partnership Goal by 2030 | Five | 5x30 Strategy |
Patient support programs for access and reimbursement
Access is a major focus, with the company reshaping the value story for customers around market access efforts. Pacira BioSciences, Inc. is seeing momentum from leading indicators that reinforce confidence in EXPAREL's sustainable growth.
- Currently estimated commercial lives with EXPAREL access: approximately 60 million
- Total covered population (commercial and government payers): nearly 90 million lives
- 5x30 Patient Reach Goal by 2030: over 3 million patients
For ZILRETTA, the company has a Patient Assist Program (PAP) that offers free medication to individuals who meet financial and other program-specific criteria.
Scientific engagement through grants and research defintely
Scientific engagement involves supporting external research and advancing the internal pipeline. Pacira BioSciences, Inc. supports medical missions and charitable initiatives by providing grants in the form of product and/or funding to registered non-profit organizations. Since 2019, the company has donated EXPAREL vials to patients in 18 countries across 5 continents.
In clinical development, the Phase 2 ASCEND study for PCRX-201 in osteoarthritis of the knee surpassed 50% enrollment in Part A as of the second quarter of 2025. This study involves approximately 135 patients. The company also acquired GQ Bio in February 2025, gaining a novel, high-capacity adenovirus vector platform for local-delivery of genetic medicines.
Finance: review Q3 2025 SG&A spend against the full-year guidance range of $310 million to $320 million by next week.
Pacira BioSciences, Inc. (PCRX) - Canvas Business Model: Channels
Direct sales force targeting surgeons and anesthesiologists
Selling, general and administrative (SG&A) expenses for the third quarter of 2025 were $91.8 million, an increase from $74.3 million in the third quarter of 2024, reflecting investments in commercial, medical, market access organization, targeted marketing initiatives, and field force expansion.
Specialty pharmaceutical distributors and wholesalers
Third quarter EXPAREL volume growth of 9 percent was partially offset by discounting associated with the launch of a new group purchasing organization (GPO) partnership, which was the third GPO launch.
Co-promotion via Johnson & Johnson MedTech sales team
Pacira BioSciences, Inc. entered a strategic collaboration with Johnson & Johnson MedTech to co-promote ZILRETTA, leveraging its specialized early intervention sales force.
ZILRETTA net product sales for the third quarter of 2025 were $29.0 million.
Hospital and Ambulatory Surgical Center (ASC) pharmacy channels
EXPAREL became eligible for separate Medicare reimbursement in both ambulatory surgical centers (ASC) and hospital outpatient (HOPD) settings beginning on January 1, 2025.
The company is ramping up reimbursement training and launching additional customer-facing materials around its new patient services hub to support adoption.
The following table details the net product sales contributing to the channel performance for the third quarter of 2025:
| Product | Q3 2025 Net Product Sales (USD) |
| EXPAREL | $139.9 million |
| ZILRETTA | $29.0 million |
| iovera° | $6.5 million |
Total revenues for the third quarter of 2025 were $179.5 million.
The full-year 2025 revenue guidance was narrowed to a range of $725 million to $735 million as of November 2025.
Pacira BioSciences, Inc. (PCRX) - Canvas Business Model: Customer Segments
You're looking at the core groups Pacira BioSciences, Inc. targets with its non-opioid pain management portfolio. Honestly, their customer base isn't one monolithic block; it's a mix of facilities, proceduralists, and the patients they treat, all centered around surgical and chronic pain episodes.
The primary commercial focus, as evidenced by their 5x30 strategy, is cementing leadership in musculoskeletal pain and adjacencies. This focus directly informs which providers and patients they prioritize.
Here's a quick look at the revenue generated by the products serving these segments through the first three quarters of 2025, which gives you a sense of where the current financial action is:
| Product | Indication Focus Area | Q1 2025 Net Product Sales | Q2 2025 Net Product Sales | Q3 2025 Net Product Sales |
| EXPAREL | Acute Post-Surgical Pain | $136.5 million | $142.9 million | $139.9 million |
| ZILRETTA | Osteoarthritis (OA) Knee Pain | $23.3 million | $31.3 million | $29.0 million |
| iovera° | Immediate/Long-Acting Drug-Free Pain Control | $5.1 million | $5.6 million | $6.5 million |
The implementation of the NOPAIN Act in January 2025 is a major tailwind, as it provides a reimbursement pathway for non-opioid products like EXPAREL and iovera° across 18 million outpatient surgical procedures, which directly impacts the facilities and proceduralists.
Hospitals and Ambulatory Surgical Centers (ASCs)
These facilities are the point of care where the majority of the product administration happens. They are critical because they manage the inventory and the reimbursement process, especially with the new J-code J0666 for EXPAREL effective January 1, 2025, streamlining billing in office settings too.
- Facilities utilizing EXPAREL for postsurgical local analgesia infiltration.
- Outpatient settings benefiting from the NOPAIN Act reimbursement pathway.
- Centers performing knee procedures where ZILRETTA is administered.
Orthopedic surgeons and sports medicine physicians
This group represents the specialists who directly prescribe or utilize the products during procedures. Their adoption drives volume for both acute and chronic pain indications.
- Surgeons using EXPAREL for various orthopedic procedures (e.g., hip, knee, foot, ankle).
- Physicians managing chronic knee pain with ZILRETTA injections.
- The total patient base treated with EXPAREL to date exceeds 15 million individuals.
Anesthesiologists and pain management specialists
These specialists are key decision-makers for regional nerve blocks and advanced pain management techniques, which is a core indication for EXPAREL and an emerging area for iovera°.
- Specialists administering EXPAREL via interscalene brachial plexus, sciatic nerve, or adductor canal blocks in adults.
- Pain specialists exploring iovera° for chronic conditions, such as the use shown in a pilot study for chronic low back pain.
- The company is advancing its pipeline, including PCRX-201, which leverages expertise in long-acting, locally administered pain therapeutics, complementary to EXPAREL.
Patients suffering from acute post-surgical pain
This is the largest patient segment driven by the flagship product, EXPAREL. The value proposition here is targeted, multi-day pain control right at the surgical site, aiming to reduce reliance on systemic opioids.
- Patients aged 6 years and older receiving EXPAREL via infiltration.
- Adult patients undergoing regional analgesia procedures.
- Patients who benefit from a single dose administered during surgery for initial post-operative pain control.
Osteoarthritis (OA) patients with knee pain
This segment is targeted specifically by ZILRETTA, an extended-release corticosteroid injection for the knee, and is a major focus for pipeline development with PCRX-201.
- Patients with OA pain of the knee receiving ZILRETTA intra-articular injections.
- The Phase 2 ASCEND study for PCRX-201, a gene therapy for OA knee pain, concluded enrollment in November 2025.
- ZILRETTA generated $29.0 million in net product sales in the third quarter of 2025.
Pacira BioSciences, Inc. (PCRX) - Canvas Business Model: Cost Structure
When you look at the cost side of Pacira BioSciences, Inc.'s business, you see a clear split between supporting the established, high-volume products and funding the transition into an innovative biopharma organization. It's a balancing act, and the numbers for 2025 show where the capital is being allocated.
High Selling, General, and Administrative (SG&A) costs are a major component, reflecting the commercial infrastructure needed to support EXPAREL and ZILRETTA. For the full year 2025, Pacira BioSciences, Inc. is guiding its Non-GAAP SG&A expense to be in the range of $310 million to $320 million. To give you a sense of the run rate, the third quarter of 2025 saw actual Non-GAAP SG&A expenses hit $91.8 million, up from $74.3 million in the third quarter of 2024. This increase is part of the investment to grow the commercial-based business.
The push toward innovation means a Significant Research and Development (R&D) investment. The updated full-year 2025 guidance for Non-GAAP R&D expense is set between $95 million and $105 million. You can see this spending in action; third-quarter 2025 R&D expenses were $26.0 million, up from $19.1 million the prior year, driven by enrollment in the PCRX-201 Phase II study and other registrational efforts.
The complexity of your core products dictates a significant portion of your cost of sales. Here's a snapshot of the cost structure elements:
| Cost Element Category | Specific Metric/Item | Latest Available Data Point (2025) |
|---|---|---|
| SG&A (Full Year Guidance) | Non-GAAP SG&A Expense | $310 million to $320 million |
| R&D (Full Year Guidance) | Non-GAAP R&D Expense | $95 million to $105 million |
| Manufacturing/COGS | Q1 2025 Cost of Goods Sold (in thousands) | $34,306 |
| Manufacturing/COGS | Q3 2025 Non-GAAP Gross Margin | 82 percent |
| Strategic Acquisition | GQ Bio Therapeutics GmbH Net Purchase Price | Approximately $32 million |
Manufacturing and cost of goods sold (COGS) for complex liposomal products is managed for efficiency, which is why the gross margin guidance is so high. The company is targeting a Non-GAAP gross margin of 80 to 82 percent for the full year 2025, benefiting from improved efficiencies in the large-scale EXPAREL manufacturing suites. For example, the Q1 2025 Cost of Goods Sold was reported at $34.3 million (in thousands, this was $34,306).
Legal and patent defense expenses for core products remain a necessary, though variable, cost. Pacira BioSciences, Inc. actively defends its intellectual property. In April 2025, the company settled litigations related to EXPAREL patents, agreeing to provide a license for generic entry starting on a confidential date in early 2030 (volume-limited) and without volume limitations beginning in 2039. Separately, in late 2025, Pacira BioSciences, Inc. filed new patent infringement lawsuits against The WhiteOak Group and Qilu Pharmaceutical to trigger a 30-month stay on FDA approval for their generic EXPAREL versions. You need to factor in the ongoing costs associated with these legal maneuvers.
The strategic acquisition of GQ Bio Therapeutics GmbH in February 2025 directly impacts the cost base by absorbing development costs and eliminating future liabilities. The net purchase price for the remaining 81% stake was approximately $32 million. What this estimate hides is the immediate financial benefit: this transaction eliminated up to $64 million in potential future milestone payments, which is a direct reduction in contingent future operating expenses.
You'll also see costs related to facility changes supporting this strategic shift:
- - Relocated corporate headquarters to Brisbane, California, in March 2025.
- - Initiated the process to wind down the Tampa training facility, expected to be offline in 2026.
- - Eliminated the EXPAREL royalty obligation, which helped boost 2025 gross margins.
Finance: draft 13-week cash view by Friday.
Pacira BioSciences, Inc. (PCRX) - Canvas Business Model: Revenue Streams
You're looking at the top-line drivers for Pacira BioSciences, Inc. as of late 2025. The company has narrowed its full-year 2025 Total Revenue Guidance to a range between $725 million and $735 million.
The core of the revenue generation comes from the sales of the key pharmaceutical products. Here's the breakdown from the most recent reported quarter, the third quarter of 2025:
| Revenue Component | Q3 2025 Net Product Sales (Millions USD) |
| Net product sales of EXPAREL | $139.9 million |
| Net product sales of ZILRETTA | $29.0 million |
| Net product sales of the iovera° system | $6.5 million |
The EXPAREL sales in the third quarter of 2025 reflected a 9 percent volume growth year-over-year, though this was partially offset by a shift in vial mix and discounting related to a new group purchasing organization (GPO) partnership. ZILRETTA net product sales were $29.0 million, up from $28.4 million in the third quarter of 2024, while iovera° sales grew to $6.5 million from $5.7 million in the prior year's third quarter.
Regarding license fees and royalties from third-party agreements, this stream is not considered a material source of consolidated revenue by Pacira BioSciences, Inc., though specific transactions do occur. For instance, sales of the bupivacaine liposome injectable suspension for veterinary use, which is tied to a licensing agreement, generated $2.6 million in the first quarter of 2025. Also, note that as of March 2025, the company stopped paying future royalties to RDF on EXPAREL sales following a legal development.
You can see the progression of the primary revenue drivers:
- Net product sales of EXPAREL (flagship product)
- Net product sales of ZILRETTA
- Net product sales of the iovera° system
- Full-year 2025 Total Revenue Guidance: $725 million to $735 million
- License fees and royalties from third-party agreements
Disclaimer
All information, articles, and product details provided on this website are for general informational and educational purposes only. We do not claim any ownership over, nor do we intend to infringe upon, any trademarks, copyrights, logos, brand names, or other intellectual property mentioned or depicted on this site. Such intellectual property remains the property of its respective owners, and any references here are made solely for identification or informational purposes, without implying any affiliation, endorsement, or partnership.
We make no representations or warranties, express or implied, regarding the accuracy, completeness, or suitability of any content or products presented. Nothing on this website should be construed as legal, tax, investment, financial, medical, or other professional advice. In addition, no part of this site—including articles or product references—constitutes a solicitation, recommendation, endorsement, advertisement, or offer to buy or sell any securities, franchises, or other financial instruments, particularly in jurisdictions where such activity would be unlawful.
All content is of a general nature and may not address the specific circumstances of any individual or entity. It is not a substitute for professional advice or services. Any actions you take based on the information provided here are strictly at your own risk. You accept full responsibility for any decisions or outcomes arising from your use of this website and agree to release us from any liability in connection with your use of, or reliance upon, the content or products found herein.