01 1M/s Dishman Carbogen Amcis Limited
02 1M/s Unilab Chemicals and Pharmaceuticals Pvt ltd
01 1Cetylpyridinium Chloride BP
02 1Cetylpyridinium Chloride BP/JP/Ph.Eur
01 1WC-0136n
02 1WC-0483
01 2India
Cetylpyridinium Chloride BP/JP/Ph.Eur
Date of Issue : 2022-09-16
Valid Till : 2025-02-07
Written Confirmation Number : WC-0136n
Address of the Firm : 1216/11,12,1216/20 to 26, G.I.D.C Estate Phase IV,Naroda, Dist -Ahmedabad-382330...
Date of Issue : 2024-04-16
Valid Till : 2027-04-16
Written Confirmation Number : WC-0483
Address of the Firm : W-32, MIDC, PHASE-II, DOMBIVLI (EAST), DOMBIVLI, Thane-421204, Maharashtra
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PharmaCompass also assists you with knowing the Cetylpyridinium Chloride API Price utilized in the formulation of products. Cetylpyridinium Chloride API Price is not always fixed or binding as the Cetylpyridinium Chloride Price is obtained through a variety of data sources. The Cetylpyridinium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Biosept manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Biosept, including repackagers and relabelers. The FDA regulates Biosept manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Biosept 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 Biosept manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Biosept supplier is an individual or a company that provides Biosept active pharmaceutical ingredient (API) or Biosept finished formulations upon request. The Biosept suppliers may include Biosept API manufacturers, exporters, distributors and traders.
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A Biosept written confirmation (Biosept WC) is an official document issued by a regulatory agency to a Biosept manufacturer, verifying that the manufacturing facility of a Biosept active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Biosept APIs or Biosept finished pharmaceutical products to another nation, regulatory agencies frequently require a Biosept WC (written confirmation) as part of the regulatory process.
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