01 1M/s. Apitoria Pharma Private Limited
01 1Ceftiofur Hydrochloride IH
01 1WC-0120
01 1India
Date of Issue : 2025-07-11
Valid Till : 2028-07-02
Written Confirmation Number : WC-0120
Address of the Firm : UNIT -I, Sy.Nos. 379, 385, 386, 388 to 396, Borpatla Village, Hathnoora Mandal, ...
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PharmaCompass offers a list of Ceftiofur 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 Ceftiofur manufacturer or Ceftiofur supplier for your needs.
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PharmaCompass also assists you with knowing the Ceftiofur API Price utilized in the formulation of products. Ceftiofur API Price is not always fixed or binding as the Ceftiofur Price is obtained through a variety of data sources. The Ceftiofur Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ceftiofur hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ceftiofur hydrochloride, including repackagers and relabelers. The FDA regulates ceftiofur hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ceftiofur hydrochloride 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 ceftiofur hydrochloride supplier is an individual or a company that provides ceftiofur hydrochloride active pharmaceutical ingredient (API) or ceftiofur hydrochloride finished formulations upon request. The ceftiofur hydrochloride suppliers may include ceftiofur hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of ceftiofur hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ceftiofur hydrochloride written confirmation (ceftiofur hydrochloride WC) is an official document issued by a regulatory agency to a ceftiofur hydrochloride manufacturer, verifying that the manufacturing facility of a ceftiofur hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting ceftiofur hydrochloride APIs or ceftiofur hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a ceftiofur hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of ceftiofur hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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