01 1M/s. Covalent Laboratories Pvt. Ltd.,
01 1Ceftibuten Hydrate JP
01 1WC-0190
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 Ceftibuten Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ceftibuten Dihydrate, including repackagers and relabelers. The FDA regulates Ceftibuten Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ceftibuten Dihydrate 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 Ceftibuten Dihydrate supplier is an individual or a company that provides Ceftibuten Dihydrate active pharmaceutical ingredient (API) or Ceftibuten Dihydrate finished formulations upon request. The Ceftibuten Dihydrate suppliers may include Ceftibuten Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Ceftibuten Dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ceftibuten Dihydrate written confirmation (Ceftibuten Dihydrate WC) is an official document issued by a regulatory agency to a Ceftibuten Dihydrate manufacturer, verifying that the manufacturing facility of a Ceftibuten Dihydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ceftibuten Dihydrate APIs or Ceftibuten Dihydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Ceftibuten Dihydrate WC (written confirmation) as part of the regulatory process.
click here to find a list of Ceftibuten Dihydrate suppliers with Written Confirmation (WC) on PharmaCompass.
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