Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
01 1M/s Apex Healthcare limited
02 1M/s Glenmark life Sciences limited
03 1M/s Optimus Drugs Pvt Ltd
04 1M/s Zydus Takeda Healthcare Pvt ltd
01 2Lornoxicam IH
02 1Lornoxicam IH/USP
03 1Lornoxicam INH
01 1WC-0182
02 1WC-0204
03 1WC-0310
04 1WC-0409
01 4India
Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
Date of Issue : 2024-03-01
Valid Till : 2026-12-31
Written Confirmation Number : WC-0409
Address of the Firm : 4710, 4711, 4707-A/8, 4707-A/9, GIDC, Industrial Estate, Ankleshwar, Dist.Bharuc...
Date of Issue : 2023-11-28
Valid Till : 2026-11-28
Written Confirmation Number : WC-0310
Address of the Firm : Plot No. Z-103/l, Dahej SEZ, Phase II, Dahej, Dist-Bharuch, Gujarat, India
Date of Issue : 2022-11-02
Valid Till : 2025-07-02
Written Confirmation Number : WC-0182
Address of the Firm : Sy.No.239&240,Dothigudem Village,Pochampally MandalYadadri-Bhuvanagiri,Dist.-508...
Date of Issue : 2022-06-15
Valid Till : 2025-07-07
Written Confirmation Number : WC-0204
Address of the Firm : C-4, MIDC, Village Pawne, Thane Belapur Road, Vashi, Navi Mumbai ? 400 703
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A Lornoxicamum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lornoxicamum, including repackagers and relabelers. The FDA regulates Lornoxicamum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lornoxicamum API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Lornoxicamum supplier is an individual or a company that provides Lornoxicamum active pharmaceutical ingredient (API) or Lornoxicamum finished formulations upon request. The Lornoxicamum suppliers may include Lornoxicamum API manufacturers, exporters, distributors and traders.
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A Lornoxicamum written confirmation (Lornoxicamum WC) is an official document issued by a regulatory agency to a Lornoxicamum manufacturer, verifying that the manufacturing facility of a Lornoxicamum active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lornoxicamum APIs or Lornoxicamum finished pharmaceutical products to another nation, regulatory agencies frequently require a Lornoxicamum WC (written confirmation) as part of the regulatory process.
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