01 1Fleming Laboratories Limited
01 1Ketotifen Hydrogen Fumarate Ph.Eur/BP
01 1WC-491n
01 1India
Ketotifen Hydrogen Fumarate Ph.Eur/BP
Date of Issue : 2024-05-07
Valid Till : 2027-04-02
Written Confirmation Number : WC-491n
Address of the Firm : Plot No. 152 & 160, Phase-V, IDA Jeedimetla, Hyderabad., Jeedimetla (V), Quthbul...
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PharmaCompass offers a list of Ketotifen Fumarate 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 Ketotifen Fumarate manufacturer or Ketotifen Fumarate supplier for your needs.
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PharmaCompass also assists you with knowing the Ketotifen Fumarate API Price utilized in the formulation of products. Ketotifen Fumarate API Price is not always fixed or binding as the Ketotifen Fumarate Price is obtained through a variety of data sources. The Ketotifen Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ketotifen fumerate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ketotifen fumerate, including repackagers and relabelers. The FDA regulates Ketotifen fumerate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ketotifen fumerate 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 Ketotifen fumerate supplier is an individual or a company that provides Ketotifen fumerate active pharmaceutical ingredient (API) or Ketotifen fumerate finished formulations upon request. The Ketotifen fumerate suppliers may include Ketotifen fumerate API manufacturers, exporters, distributors and traders.
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A Ketotifen fumerate written confirmation (Ketotifen fumerate WC) is an official document issued by a regulatory agency to a Ketotifen fumerate manufacturer, verifying that the manufacturing facility of a Ketotifen fumerate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ketotifen fumerate APIs or Ketotifen fumerate finished pharmaceutical products to another nation, regulatory agencies frequently require a Ketotifen fumerate WC (written confirmation) as part of the regulatory process.
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