01 1M/s. Avik Pharmaceutical Limited
01 1Clobetasol Butyrate BP/EP
01 1WC-0169
01 1India
Date of Issue : 2019-06-27
Valid Till : 2022-07-02
Written Confirmation Number : WC-0169
Address of the Firm : A-1/7, 1st Phase GIDC, Vapi-396 195, Valsad, Gujarat, India
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PharmaCompass offers a list of Clobetasol Butyrate 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 Clobetasol Butyrate manufacturer or Clobetasol Butyrate supplier for your needs.
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PharmaCompass also assists you with knowing the Clobetasol Butyrate API Price utilized in the formulation of products. Clobetasol Butyrate API Price is not always fixed or binding as the Clobetasol Butyrate Price is obtained through a variety of data sources. The Clobetasol Butyrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Clobetasol Butyrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clobetasol Butyrate, including repackagers and relabelers. The FDA regulates Clobetasol Butyrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clobetasol Butyrate 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 Clobetasol Butyrate supplier is an individual or a company that provides Clobetasol Butyrate active pharmaceutical ingredient (API) or Clobetasol Butyrate finished formulations upon request. The Clobetasol Butyrate suppliers may include Clobetasol Butyrate API manufacturers, exporters, distributors and traders.
click here to find a list of Clobetasol Butyrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Clobetasol Butyrate written confirmation (Clobetasol Butyrate WC) is an official document issued by a regulatory agency to a Clobetasol Butyrate manufacturer, verifying that the manufacturing facility of a Clobetasol Butyrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Clobetasol Butyrate APIs or Clobetasol Butyrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Clobetasol Butyrate WC (written confirmation) as part of the regulatory process.
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