01 1M/s. Sun Pharmaceuticals Industries Ltd.
01 1Disodium Pamidronate (USP/EP/BP)
01 1WC-0159
01 1India
Disodium Pamidronate (USP/EP/BP)
Date of Issue : 2022-06-08
Valid Till : 2025-07-25
Written Confirmation Number : WC-0159
Address of the Firm : A-7/A-8, MIDC, Ahmednagar-414 111, Maharashtra State
69
PharmaCompass offers a list of Pamidronate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Pamidronate manufacturer or Pamidronate supplier for your needs.
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A Disodium Pamidronate Pentahydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disodium Pamidronate Pentahydrate, including repackagers and relabelers. The FDA regulates Disodium Pamidronate Pentahydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Disodium Pamidronate Pentahydrate 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 Disodium Pamidronate Pentahydrate supplier is an individual or a company that provides Disodium Pamidronate Pentahydrate active pharmaceutical ingredient (API) or Disodium Pamidronate Pentahydrate finished formulations upon request. The Disodium Pamidronate Pentahydrate suppliers may include Disodium Pamidronate Pentahydrate API manufacturers, exporters, distributors and traders.
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A Disodium Pamidronate Pentahydrate written confirmation (Disodium Pamidronate Pentahydrate WC) is an official document issued by a regulatory agency to a Disodium Pamidronate Pentahydrate manufacturer, verifying that the manufacturing facility of a Disodium Pamidronate Pentahydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Disodium Pamidronate Pentahydrate APIs or Disodium Pamidronate Pentahydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Disodium Pamidronate Pentahydrate WC (written confirmation) as part of the regulatory process.
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