Médicaments

Wholesale Generic Drugs & Medicines

Pharmint: A Trusted B2B Marketplace for Bulk Generic Pharmaceuticals

Pharmint powers a B2B pharmaceutical marketplace that enables healthcare providers, pharmacies, and procurement organizations to source FDA-approved generic drugs, APIs, and OTC medicines from verified GMP-certified manufacturers across global markets.

Your Gateway to Trusted Generic Medicine Suppliers

We simplify sourcing with a unified platform featuring:

• Generic Tablets, Capsules, Injectables, and Specialty Generics
• Over-the-Counter (OTC) Pharmaceuticals for retail & clinical settings
• Bulk APIs from compliant manufacturers across India, EU, and LATAM
• Support for both prescription and hospital-grade medicines

All suppliers are validated for GMP compliance, regulatory dossier access (CTD/ACTD), and real-world distribution capacity.

Generic Drug Manufacturing & Supply

✅ Verified Pharmaceutical Manufacturers

We partner with WHO-GMP, USFDA, and EU-GMP certified manufacturers to ensure safety, consistency, and compliance. Every supplier on Pharmint is thoroughly vetted and required to maintain strict documentation across CTD formats, stability data, and bioequivalence studies.

Wholesale Procurement Process

1. Discover medications by filtering dossiers by dosage form, country of origin, and approval status.
2. Compare supplier quotes in real-time.
3. Negotiate terms, pricing, and MOQ with direct manufacturer access.
4. Secure the transaction with escrow-backed, compliance-verified procurement.

Escrow-Backed Trade System & Risk-Free Procurement

Buyers enjoy unmatched confidence via:

• Escrow-secured payments held until delivery verification
  
• Full traceability from manufacturer to port
  
• Verified supplier documents (GMP, CEP, FDA, WHO PQ certifications)
  

CTD Dossiers & Regulatory Intelligence at Scale

Discover qualified generics by:

• Country of origin
  
• Dossier availability (CTD, ACTD, EU Module 1)
  
• Therapeutic classification: anti-infectives, cardiovascular, CNS, anti-diabetic
  
• ICH zone stability, BA/BE study access
  

Our expert-curated database enables regulatory-aligned product discovery in minutes.

For Wholesalers, Pharmacies & Hospital Buyers

Pharmint supports:

• Retail Pharmacies: MOQ-friendly sourcing and formulary cost optimization
  
• Hospital Procurement Teams: Injectable-focused distribution and cold-chain logistics
  
• Pharmaceutical Wholesalers: Margin-optimized generics from private-label and direct manufacturers
  
• Distributors and CMOs: Inventory synchronization and automated RFQ management
  

Why Choose Pharmint as Your Generic Drug Partner?

• Access to 10,000+ active SKUs across key molecules
  
• Network of 500+ GMP-certified manufacturers
  
• Advanced search by API strength, form, and packaging
  
• Private-label generics for brand-agnostic expansion
  
• End-to-end support for regulatory filings and technical data

Wholesale Generic Drugs & Medicines FAQs

How do I verify if a generic drug supplier is GMP-certified?

To verify GMP certification, buyers can request official audit reports or GMP certificates from the supplier; regulatory bodies like the USFDA, WHO, and EMA maintain public GMP registries.

Can I import generic drugs without a local marketing authorization?

No, importing generic drugs typically requires local marketing authorization or temporary import permits, depending on national regulations; Pharmint provides dossier mapping for compliant import.

Are private-label generic drugs allowed for international resale?

Yes, private-label generics are permitted for resale if regulatory-compliant; buyer must ensure brand labeling, GMP equivalency, and export/import licensing are aligned with target market laws.

What’s the difference between CTD and eCTD formats in pharma?

CTD is the structured dossier format for drug approval; eCTD is its digital, submission-ready version required by many regulatory agencies for electronic filing.

What documents are needed to import generic medicines?

You’ll need a GMP certificate, CTD dossier, product CoA, and an import license or marketing authorization; Pharmint validates and aligns these with your regulatory body.