WHO-GMP Certified Commercial Supply

VEERIX-AMOXYCILLIN Capsules Contract Manufacturing & CDMO

Veerix Biotech is a WHO-GMP certified third-party pharmaceutical manufacturer and CDMO partner producing VEERIX-AMOXYCILLIN Capsules (AMOXYCILLIN TRIHYDRATE IP EQ. TO AMOXYCILLIN & POTASSIUM CLAVULANATE DILUTED IP EQ. TO CLAVULANIC ACID SUSPENSION) within the Anti Infectives therapeutic class, with complete Certificate of Analysis (CoA), stability studies, and regulatory dossier compliance for domestic Indian and global export markets.

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Technical Specifications & Formulation Details

Product NameVEERIX-AMOXYCILLIN Capsules
Active CompositionAMOXYCILLIN TRIHYDRATE IP EQ. TO AMOXYCILLIN & POTASSIUM CLAVULANATE DILUTED IP EQ. TO CLAVULANIC ACID SUSPENSION
Therapeutic SegmentAnti Infectives
Dosage FormCapsules
Primary Packaging10*10 Capsules
Quality StandardIP / BP / USP Pharmacopeial Standard, WHO-GMP Certified
Manufacturing FacilityTahliwal Industrial Area, Tehsil Haroli, Una, Himachal Pradesh & Coimbatore, Tamil Nadu
Regulatory DocumentationBatch Release CoA, Method of Analysis (MOA), Accelerated & Real-time Stability Data, CTD Module 3

Commercial Supply Capabilities for VEERIX-AMOXYCILLIN Capsules

Veerix Biotech provides end-to-end commercial supply and technical scoping for VEERIX-AMOXYCILLIN Capsules in the Anti Infectives class. From pre-formulation screening and pilot batch validation to automated blister packaging, serialisation, and multi-market regulatory clearance, our direct facilities and audited partner network ensure seamless execution.

  • Custom private label packaging with brand foil printing and anti-counterfeit features
  • Batch volume scalability: from pilot validation batches to large-scale commercial export runs
  • Dedicated QA/QC release testing including HPLC assay, dissolution testing, and microbial limits
  • Strict confidentiality with mutual non-disclosure agreement (NDA) upfront
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