01 1Solara Active Pharma Sciences Limited
01 1Ranitidine IH
01 1WC-0127
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
55
PharmaCompass offers a list of Ranitidine 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 Ranitidine manufacturer or Ranitidine supplier for your needs.
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PharmaCompass also assists you with knowing the Ranitidine API Price utilized in the formulation of products. Ranitidine API Price is not always fixed or binding as the Ranitidine Price is obtained through a variety of data sources. The Ranitidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vizerul manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vizerul, including repackagers and relabelers. The FDA regulates Vizerul manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vizerul 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 Vizerul manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vizerul supplier is an individual or a company that provides Vizerul active pharmaceutical ingredient (API) or Vizerul finished formulations upon request. The Vizerul suppliers may include Vizerul API manufacturers, exporters, distributors and traders.
click here to find a list of Vizerul suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vizerul written confirmation (Vizerul WC) is an official document issued by a regulatory agency to a Vizerul manufacturer, verifying that the manufacturing facility of a Vizerul active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Vizerul APIs or Vizerul finished pharmaceutical products to another nation, regulatory agencies frequently require a Vizerul WC (written confirmation) as part of the regulatory process.
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