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01 1M/s. Covalent Laboratories Pvt. Ltd.,
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01 1Ceftibuten Hydrate JP
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01 1WC-0190
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01 1India
Date of Issue : 2019-09-03
Valid Till : 2022-09-03
Written Confirmation Number : WC-0190
Address of the Firm : Sy.No.374, Gundla Machanoor Village, Hathnoor Mandal, Medak District-502 296, AP
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PharmaCompass offers a list of Ceftibuten Dihydrate 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 Ceftibuten Dihydrate manufacturer or Ceftibuten Dihydrate supplier for your needs.
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PharmaCompass also assists you with knowing the Ceftibuten Dihydrate API Price utilized in the formulation of products. Ceftibuten Dihydrate API Price is not always fixed or binding as the Ceftibuten Dihydrate Price is obtained through a variety of data sources. The Ceftibuten Dihydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CEDAX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CEDAX, including repackagers and relabelers. The FDA regulates CEDAX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CEDAX 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 CEDAX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CEDAX supplier is an individual or a company that provides CEDAX active pharmaceutical ingredient (API) or CEDAX finished formulations upon request. The CEDAX suppliers may include CEDAX API manufacturers, exporters, distributors and traders.
click here to find a list of CEDAX suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CEDAX written confirmation (CEDAX WC) is an official document issued by a regulatory agency to a CEDAX manufacturer, verifying that the manufacturing facility of a CEDAX active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting CEDAX APIs or CEDAX finished pharmaceutical products to another nation, regulatory agencies frequently require a CEDAX WC (written confirmation) as part of the regulatory process.
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