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How to Source Pregabalin Capsule for Pharmaceutical Formulation

Pregabalin Capsule (Capsules, 25 mg, 50 mg, 75 mg, 100 mg, 150 mg, 200 mg, 225 mg, 300 mg) is classified under Antipsychotropic Drugs. It is therapeutically aligned with reference brands such as Lyrica(US & EU). This guide highlights key sourcing factors buyers should consider when procuring high-quality Pregabalin Capsule for formulation, R&D, or bulk manufacturing.

Product Overview: Pregabalin, marketed as Lyrica, is available in capsules, oral solution, and extended-release tablets across US and EU markets. Indicated for neuropathic pain, epilepsy, and anxiety, it offers consistent demand. An essential listing for CNS-focused pharma B2B platforms aiming for global regulated markets. Pregabalin is an antiepileptic and neuropathic pain agent approved for conditions like fibromyalgia,...

Pregabalin Capsule API in Capsules form, 25 mg, 50 mg, 75 mg, 100 mg, 150 mg, 200 mg, 225 mg, 300 mg specification
Pregabalin Capsule API – ideal for compliant pharmaceutical formulation.
Quick Insight: Over 60% of formulation delays are linked to poor API sourcing. A well-planned sourcing strategy can reduce risk and accelerate market entry.

1. Regulatory Compliance & Documentation

Ensure suppliers provide:

2. Purity, Grade & Specification Matching

Pregabalin Capsule must meet exact grade and purity for your dosage form:

3. Supplier Reliability & Audit History

4. Commercial Terms: Pricing, MOQ & Flexibility

5. Lead Time, Inventory & Logistics

Typical lead time for Pregabalin Capsule is 4–6 weeks.

6. Formulation Support

Pro Tip: Engage supplier formulation experts early — it can improve bioavailability and cut development time.

Conclusion

Sourcing Pregabalin Capsule is more than procurement—it’s a strategic partnership. With its capsules form and 25 mg, 50 mg, 75 mg, 100 mg, 150 mg, 200 mg, 225 mg, 300 mg 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 Pregabalin Capsule.

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Frequently Asked Questions For Sourcing of Pregabalin Capsule

What is the typical lead time for Pregabalin Capsule?

Lead times range from 4–6 weeks depending on supplier and region.

Is Pregabalin Capsule available in multiple grades?

Yes — common grades include USP, EP, and JP. Verify grade suitability for your dosage form before purchase.

Does Pregabalin Capsule require special storage?

It should be stored in a cool, dry place away from direct sunlight.

Is a Drug Master File (DMF) available for Pregabalin Capsule?

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 Pregabalin Capsule?

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 Pregabalin Capsule?

Available documentation may include GMP, ISO 9001, ISO 14001, and ICH Q7 certificates, along with CoA, TDS, and stability data.

Is Pregabalin Capsule suitable for regulated markets like US/EU?

Yes — compliant with EU/US/WHO GMP standards and available with regulatory support documentation for filings.

Can Pregabalin Capsule 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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