Maithri Drugs: Dedicated to your API needs.
01 1M/sMaithri laboratories Private Limited
02 1M/sSurajlok Chemicals Pvt. Ltds
01 1Pyridostigmine Bromide BP
02 1Pyridostigmine Bromide USP/EP
01 1WC-0435
02 1WC-0455
01 2India
Maithri Drugs: Dedicated to your API needs.
Date of Issue : 2026-02-24
Valid Till : 2029-02-23
Written Confirmation Number : WC-0455
Address of the Firm : Sy No. 14, IDA Gaddapotharam, Gaddapotharam (V), Jinnaram (M), Sangareddy (D), T...
Date of Issue : 2025-10-08
Valid Till : 2028-10-07
Written Confirmation Number : WC-0435
Address of the Firm : Plot No. T-6, M.I.D.C, Tarapur Industrial Area, Boisar, Dist-Thane -401506 Mahar...
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A DSSTox_RID_77069 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_RID_77069, including repackagers and relabelers. The FDA regulates DSSTox_RID_77069 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_RID_77069 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 DSSTox_RID_77069 supplier is an individual or a company that provides DSSTox_RID_77069 active pharmaceutical ingredient (API) or DSSTox_RID_77069 finished formulations upon request. The DSSTox_RID_77069 suppliers may include DSSTox_RID_77069 API manufacturers, exporters, distributors and traders.
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A DSSTox_RID_77069 written confirmation (DSSTox_RID_77069 WC) is an official document issued by a regulatory agency to a DSSTox_RID_77069 manufacturer, verifying that the manufacturing facility of a DSSTox_RID_77069 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting DSSTox_RID_77069 APIs or DSSTox_RID_77069 finished pharmaceutical products to another nation, regulatory agencies frequently require a DSSTox_RID_77069 WC (written confirmation) as part of the regulatory process.
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