WHO-GMP Certified Commercial Supply

VEERIX-FLUPIRTINE Tablets Contract Manufacturing & CDMO

Veerix Biotech is a WHO-GMP certified third-party pharmaceutical manufacturer and CDMO partner producing VEERIX-FLUPIRTINE Tablets (FLUPIRTINE MALEATE, PARACETAMOL IP UNCOATED BILAYERED TABLET) within the Pain Analgesics 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-FLUPIRTINE Tablets
Active CompositionFLUPIRTINE MALEATE, PARACETAMOL IP UNCOATED BILAYERED TABLET
Therapeutic SegmentPain Analgesics
Dosage FormTablets
Primary Packaging10*10 Tablets
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-FLUPIRTINE Tablets

Veerix Biotech provides end-to-end commercial supply and technical scoping for VEERIX-FLUPIRTINE Tablets in the Pain Analgesics 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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