01 1M/s Kumar Organic Products Limited
01 1Ciclopiroxolamine USP
01 1WC-0238
01 1India
Date of Issue : 2024-02-08
Valid Till : 2027-01-28
Written Confirmation Number : WC-0238
Address of the Firm : Plot No. 60/65, 62 and 64 Road No. 3 & 5, Jigani Industrial Area, Anekal Taluk, ...
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PharmaCompass offers a list of Ciclopirox Olamine 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 Ciclopirox Olamine manufacturer or Ciclopirox Olamine supplier for your needs.
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PharmaCompass also assists you with knowing the Ciclopirox Olamine API Price utilized in the formulation of products. Ciclopirox Olamine API Price is not always fixed or binding as the Ciclopirox Olamine Price is obtained through a variety of data sources. The Ciclopirox Olamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Brumixol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Brumixol, including repackagers and relabelers. The FDA regulates Brumixol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Brumixol 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 Brumixol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Brumixol supplier is an individual or a company that provides Brumixol active pharmaceutical ingredient (API) or Brumixol finished formulations upon request. The Brumixol suppliers may include Brumixol API manufacturers, exporters, distributors and traders.
click here to find a list of Brumixol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Brumixol written confirmation (Brumixol WC) is an official document issued by a regulatory agency to a Brumixol manufacturer, verifying that the manufacturing facility of a Brumixol active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Brumixol APIs or Brumixol finished pharmaceutical products to another nation, regulatory agencies frequently require a Brumixol WC (written confirmation) as part of the regulatory process.
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