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 Dishman Carbogen Amcis Limiteds
03 1M/s Ipca Laboratories Ltd
01 1Benzocaine BP/EP/USP
02 1Benzocaine BP/Ph.Eur/USP
03 1Benzocaine BP/USP/Ph.Eur.
01 1WC-0135
02 1WC-0409
03 1WC-0453
01 3India
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 : 2022-09-30
Valid Till : 2025-06-30
Written Confirmation Number : WC-0135
Address of the Firm : Survey No.47,48 Paiki sub Plot No.1, Village Lodariyal, Tal -Sanand, Dist -Ahmed...
Date of Issue : 2023-09-25
Valid Till : 2026-03-20
Written Confirmation Number : WC-0453
Address of the Firm : Plot NO.E-41,129&128/2, MIDCInd.Area,Tarapur,Boisar-401 506, Maharashtra, India
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A Anaesthesinum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anaesthesinum, including repackagers and relabelers. The FDA regulates Anaesthesinum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anaesthesinum 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 Anaesthesinum supplier is an individual or a company that provides Anaesthesinum active pharmaceutical ingredient (API) or Anaesthesinum finished formulations upon request. The Anaesthesinum suppliers may include Anaesthesinum API manufacturers, exporters, distributors and traders.
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A Anaesthesinum written confirmation (Anaesthesinum WC) is an official document issued by a regulatory agency to a Anaesthesinum manufacturer, verifying that the manufacturing facility of a Anaesthesinum active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Anaesthesinum APIs or Anaesthesinum finished pharmaceutical products to another nation, regulatory agencies frequently require a Anaesthesinum WC (written confirmation) as part of the regulatory process.
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