01 1M/s IPCA Laboratories Ltd
02 1M/s Unichem Laboratories Limited
01 1Bendroflumethiazide BP/Ph.Eur.
02 1Bendroflumethiazide Ph.Eur
01 1WC-0063
02 1WC-0091n
01 2India
Bendroflumethiazide BP/Ph.Eur.
Date of Issue : 2022-06-08
Valid Till : 2025-07-02
Written Confirmation Number : WC-0091n
Address of the Firm : P.O. Sejavta, Dist. Ratlam, Madhya Pradesh, India.
Date of Issue : 2022-06-30
Valid Till : 2025-07-28
Written Confirmation Number : WC-0063
Address of the Firm : Plot No. 99, MIDC Area - Dhatav Roha, Dist. Raigad, Roha, Raigad-402116, Maharas...
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A Prestwick3_000784 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000784, including repackagers and relabelers. The FDA regulates Prestwick3_000784 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000784 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 Prestwick3_000784 supplier is an individual or a company that provides Prestwick3_000784 active pharmaceutical ingredient (API) or Prestwick3_000784 finished formulations upon request. The Prestwick3_000784 suppliers may include Prestwick3_000784 API manufacturers, exporters, distributors and traders.
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A Prestwick3_000784 written confirmation (Prestwick3_000784 WC) is an official document issued by a regulatory agency to a Prestwick3_000784 manufacturer, verifying that the manufacturing facility of a Prestwick3_000784 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Prestwick3_000784 APIs or Prestwick3_000784 finished pharmaceutical products to another nation, regulatory agencies frequently require a Prestwick3_000784 WC (written confirmation) as part of the regulatory process.
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