01 1M/s Symbiotec Pharmalab Pvt Ltd
02 1M/s Symbiotec Pharmalab Pvt ltd
03 1M/sAvik Pharmaceuticals Limited
01 2Clobetasone Butyrate BP/EP
02 1Clobetasone Butyrate EP/BP
01 1WC-0161A
02 1WC-0161n
03 1WC-0169
01 3India
Date of Issue : 2022-07-15
Valid Till : 2025-07-02
Written Confirmation Number : WC-0169
Address of the Firm : Plot no. A-1/7 & A-1/8, 1st Phase G.I.D.C Vapi, Valsad-396195, Gujarat India
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A
Address of the Firm : 385/2, Gram Pigdamber, Rau , Indore-453331, Madhya Pradesh, India
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161n
Address of the Firm : PLOT NO.385/2, Gram Pigdamber, Rau , Indore-453331, Madhya Pradesh, India
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PharmaCompass offers a list of Clobetasone 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 Clobetasone Butyrate manufacturer or Clobetasone Butyrate supplier for your needs.
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A Clobetasone 17-Butyrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clobetasone 17-Butyrate, including repackagers and relabelers. The FDA regulates Clobetasone 17-Butyrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clobetasone 17-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 Clobetasone 17-Butyrate supplier is an individual or a company that provides Clobetasone 17-Butyrate active pharmaceutical ingredient (API) or Clobetasone 17-Butyrate finished formulations upon request. The Clobetasone 17-Butyrate suppliers may include Clobetasone 17-Butyrate API manufacturers, exporters, distributors and traders.
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A Clobetasone 17-Butyrate written confirmation (Clobetasone 17-Butyrate WC) is an official document issued by a regulatory agency to a Clobetasone 17-Butyrate manufacturer, verifying that the manufacturing facility of a Clobetasone 17-Butyrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Clobetasone 17-Butyrate APIs or Clobetasone 17-Butyrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Clobetasone 17-Butyrate WC (written confirmation) as part of the regulatory process.
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