WHO-GMP Certified Commercial Supply

VEERIX-DICLOFENAC Cream Contract Manufacturing & CDMO

Veerix Biotech is a WHO-GMP certified third-party pharmaceutical manufacturer and CDMO partner producing VEERIX-DICLOFENAC Cream (DICLOFENAC DIETHYLAMINE IP 1.16% W/W EQ. TO DICLOFENAC SODIUM 1% W/W METHYL SALICYLATE IP 10% 1.16% W/W 1% W/W10% W/W MENTHOL IP 5% W/W LINSEED OIL BP 3% W/W THIOCOLCHICOSIDE IP 0.125% BENZYL ALCOHOL (AS W/W5% W/W 3% W/W0.125% PRESERVATIVE) IP 1% W/W GEL BASE Q.S) 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-DICLOFENAC Cream
Active CompositionDICLOFENAC DIETHYLAMINE IP 1.16% W/W EQ. TO DICLOFENAC SODIUM 1% W/W METHYL SALICYLATE IP 10% 1.16% W/W 1% W/W10% W/W MENTHOL IP 5% W/W LINSEED OIL BP 3% W/W THIOCOLCHICOSIDE IP 0.125% BENZYL ALCOHOL (AS W/W5% W/W 3% W/W0.125% PRESERVATIVE) IP 1% W/W GEL BASE Q.S
Therapeutic SegmentPain Analgesics
Dosage FormOintments
Primary Packaging15g / 30g
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-DICLOFENAC Cream

Veerix Biotech provides end-to-end commercial supply and technical scoping for VEERIX-DICLOFENAC Cream 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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