Pregabalin Suppliers & Bulk Manufacturers
Available Forms: Extended-Release Tablets
Available Strengths: 82.5 mg, 165 mg, 330 mg
Reference Brands: Lyrica(US & EU)
Category: Antipsychotropic Drugs
Pregabalin is available in Extended-Release Tablets and strengths such as 82.5 mg, 165 mg, 330 mg. Sourced from GMP-certified and ISO-compliant manufacturers, this API meets global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical formulation and commercial manufacturing, Pregabalin is supplied in bulk quantities with complete regulatory support including DMF, COA, and MSDS.
| Technical Specifications & Supply Details | |
|---|---|
| Lead Time | 7 to 60 days (depending on batch size & schedule) |
| MOQ | As per manufacturer’s batch size |
| COA | Available with every batch |
| Regulatory Dossier / DMF | Available upon request |
| Export Documentation | FSC, COA, Manufacturing License, Product Permission |
| Standards | IP, BP, USP |
| Certifications | WHO-GMP, EU-GMP, USFDA (as applicable) |
Pregabalin can be exported to over 30 countries across Asia, Africa, Europe, and Latin America. Flexible packaging, competitive pricing, and a verified supplier network make Pharmatradz a trusted sourcing partner for pharmaceutical companies and contract manufacturers worldwide.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
Product Description: Pregabalin is an antiepileptic and neuropathic pain agent approved for conditions like fibromyalgia, diabetic neuropathy, postherpetic neuralgia, and generalized anxiety disorder. It is commercially available in oral capsule (25–300 mg), oral solution (20 mg/mL), and extended-release tablet (82.5–330 mg) formats. Marketed under the brand Lyrica by Pfizer in the US and EU, it is also widely available as a generic. Pregabalin is a high-demand CNS product due to its therapeutic versatility. Pharma B2B suppliers targeting neurology, pain management, and psychiatric markets find Pregabalin a key listing for regulated pharmaceutical export and commercial distribution in the US and European regions.
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