How to Source Nepafenac for Pharmaceutical Formulation
Nepafenac (Eye Drops, 0.1%, 0.3%) is classified under Opthalmology. It is therapeutically aligned with reference brands such as Nevanac (USA/EU), Ilevro (USA/EU). This guide highlights key sourcing factors buyers should consider when procuring high-quality Nepafenac for formulation, R&D, or bulk manufacturing.
Product Overview:
Nepafenac is available as ophthalmic suspension in strengths 0.1% and 0.3%, supplied in sterile dropper bottles for ocular use.
Short description: Nepafenac is a nonsteroidal anti-inflammatory drug used in the eye to reduce pain and inflammation associated with cataract surgery. It is a prodrug that converts to amfenac in ocular tissues, providing targeted anti-inflammatory effects. It is usually prescribed for short-term postoperative management.
1. Regulatory Compliance & Documentation
Ensure suppliers provide:
- ✔ Valid DMF (Drug Master File)
- ✔ COA (Certificate of Analysis) for each batch
- ✔ GMP, ISO, or ICH Q7 compliance certificates
2. Purity, Grade & Specification Matching
Nepafenac must meet exact grade and purity for your dosage form:
- ✔ USP / EP / JP grade verification
- ✔ Particle size distribution check
- ✔ Residual solvent and heavy metal limits
3. Supplier Reliability & Audit History
- ✔ Positive past audit reports
- ✔ Pharma client references
- ✔ Years of proven API manufacturing experience
4. Commercial Terms: Pricing, MOQ & Flexibility
- ✔ Transparent pricing
- ✔ Pilot batch MOQ flexibility
- ✔ Volume-based discounts
5. Lead Time, Inventory & Logistics
Typical lead time for Nepafenac is 4–6 weeks.
- ✔ Emergency dispatch options
- ✔ Regional warehousing
- ✔ Special storage if needed
6. Formulation Support
- ✔ Technical datasheets
- ✔ Sample availability
- ✔ Stability study support
Conclusion
Sourcing Nepafenac is more than procurement—it’s a strategic partnership. With its eye drops form and 0.1%, 0.3% specification, choosing a compliant supplier ensures consistent quality and regulatory approval. Prioritize documentation, verify compatibility, and build relationships with transparent, reliable suppliers to secure long-term success.
Next Step: Get expert assistance in sourcing Nepafenac.
Frequently Asked Questions For Sourcing of Nepafenac
What is the typical lead time for Nepafenac?
Lead times range from 4–6 weeks depending on supplier and region.
Is Nepafenac available in multiple grades?
Yes — common grades include USP, EP, and JP. Verify grade suitability for your dosage form before purchase.
Does Nepafenac require special storage?
It should be stored in a cool, dry place away from direct sunlight.
Is a Drug Master File (DMF) available for Nepafenac?
Yes, a DMF is available for regulated markets upon request. It includes detailed quality, manufacturing, and stability data.
Can I request samples or a pilot batch of Nepafenac?
Yes — pilot batches or samples can be arranged for R&D, stability studies, or formulation trials. MOQ may vary based on region and regulatory scope.
What compliance certificates are available for Nepafenac?
Available documentation may include GMP, ISO 9001, ISO 14001, and ICH Q7 certificates, along with CoA, TDS, and stability data.
Is Nepafenac suitable for regulated markets like US/EU?
Yes — compliant with EU/US/WHO GMP standards and available with regulatory support documentation for filings.
Can Nepafenac be used in fixed-dose combinations?
Yes — many formulations support inclusion in FDCs. Compatibility studies and formulation consultation are available on request.
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