Maithri Drugs: Dedicated to your API needs.
01 1M/s Maithri Drugs Private Limited
01 1Sodium sulphate anhydrous IH/USP/EP
01 1WC-0407
01 1India
Maithri Drugs: Dedicated to your API needs.
Sodium sulphate anhydrous IH/USP/EP
Date of Issue : 2024-02-12
Valid Till : 2027-02-11
Written Confirmation Number : WC-0407
Address of the Firm : Sy. No. 205, 222 to 226, IDA Bonthapally, Bonthapally (Village), Gummadidala (Ma...
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A SODIUM SULFATE ANHYDROUS manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SODIUM SULFATE ANHYDROUS, including repackagers and relabelers. The FDA regulates SODIUM SULFATE ANHYDROUS manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SODIUM SULFATE ANHYDROUS API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of SODIUM SULFATE ANHYDROUS manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A SODIUM SULFATE ANHYDROUS supplier is an individual or a company that provides SODIUM SULFATE ANHYDROUS active pharmaceutical ingredient (API) or SODIUM SULFATE ANHYDROUS finished formulations upon request. The SODIUM SULFATE ANHYDROUS suppliers may include SODIUM SULFATE ANHYDROUS API manufacturers, exporters, distributors and traders.
click here to find a list of SODIUM SULFATE ANHYDROUS suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A SODIUM SULFATE ANHYDROUS written confirmation (SODIUM SULFATE ANHYDROUS WC) is an official document issued by a regulatory agency to a SODIUM SULFATE ANHYDROUS manufacturer, verifying that the manufacturing facility of a SODIUM SULFATE ANHYDROUS active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting SODIUM SULFATE ANHYDROUS APIs or SODIUM SULFATE ANHYDROUS finished pharmaceutical products to another nation, regulatory agencies frequently require a SODIUM SULFATE ANHYDROUS WC (written confirmation) as part of the regulatory process.
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