Taj Pharma operates a dedicated Fenbendazole manufacturing block in Vapi, Gujarat, with segregated HVAC zones, automated process controls, and digital batch tracking. The facility supports multiple strengths (222mg, 444mg, 500mg, 1000mg) with high-volume capacity and stringent quality oversight.
Tablets per day capacity
Max batch size (tablets)
Compression stations across lines
Countries with technical transfers
Our manufacturing facility is certified under WHO-GMP standards, ensuring compliance with global quality requirements for pharmaceutical production.
Certificate Number: WHO-GMP/IND/2023/001
Valid Until: December 31, 2025
Certified By: World Health Organization
Scope: Fenbendazole Tablets Manufacturing
Compliance: WHO Good Manufacturing Practices for Pharmaceutical Products
EP/USP/BP compliant APIs and excipients with Vendor Qualification & COA verification.
Validated blending times, sieve checks, and moisture control with IPC records.
Tablet hardness, thickness, and friability checks per SOP; in-process dissolution trending.
Line clearance, vision inspection, tamper seals, and optional serialization/aggregation.
QA summary report, COA issuance, stability placement, and retain sample storage.
For prescription and export purposes only. Use under medical supervision. Not intended for self-medication. Information for educational purposes. Export subject to local regulations.
© 2026 Fenbendazole Pharma. All Rights Reserved.
For prescription and export purposes only. Not intended for self-medication. Export subject to local regulations.