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01 1Solara Active Pharma Sciences Limited
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01 1Ranitidine IH
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01 1WC-0127
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01 1India
Date of Issue : 2022-09-30
Valid Till : 2025-08-04
Written Confirmation Number : WC-0127
Address of the Firm : A1/B, SIPCOT Industrial Complex, Kudikadu, Cuddalore-607 005
A Ranitidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ranitidine, including repackagers and relabelers. The FDA regulates Ranitidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ranitidine 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 Ranitidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ranitidine supplier is an individual or a company that provides Ranitidine active pharmaceutical ingredient (API) or Ranitidine finished formulations upon request. The Ranitidine suppliers may include Ranitidine API manufacturers, exporters, distributors and traders.
click here to find a list of Ranitidine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ranitidine written confirmation (Ranitidine WC) is an official document issued by a regulatory agency to a Ranitidine manufacturer, verifying that the manufacturing facility of a Ranitidine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ranitidine APIs or Ranitidine finished pharmaceutical products to another nation, regulatory agencies frequently require a Ranitidine WC (written confirmation) as part of the regulatory process.
click here to find a list of Ranitidine suppliers with Written Confirmation (WC) on PharmaCompass.
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