01 1M/s IPCA Laboratories Ltd
01 1Metoclopramide Base BP/Ph.Eur./JP
01 1WC-0091n
01 1India
Metoclopramide Base BP/Ph.Eur./JP
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.
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A C14H22ClN3O2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C14H22ClN3O2, including repackagers and relabelers. The FDA regulates C14H22ClN3O2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C14H22ClN3O2 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 C14H22ClN3O2 supplier is an individual or a company that provides C14H22ClN3O2 active pharmaceutical ingredient (API) or C14H22ClN3O2 finished formulations upon request. The C14H22ClN3O2 suppliers may include C14H22ClN3O2 API manufacturers, exporters, distributors and traders.
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A C14H22ClN3O2 written confirmation (C14H22ClN3O2 WC) is an official document issued by a regulatory agency to a C14H22ClN3O2 manufacturer, verifying that the manufacturing facility of a C14H22ClN3O2 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting C14H22ClN3O2 APIs or C14H22ClN3O2 finished pharmaceutical products to another nation, regulatory agencies frequently require a C14H22ClN3O2 WC (written confirmation) as part of the regulatory process.
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