01 2M/s Lupin Limited
02 2M/s. Apitoria Pharma Private Limited
01 1Cefadroxil Monohydrate BP/Ph. Eur
02 1Cefadroxil Monohydrate Ph. Eur
03 1Cefadroxil Monohydrate Ph.Eur
04 1Cefadroxil USP
01 1WC-0023
02 2WC-0048
03 1WC-0120
01 4India
Date of Issue : 07-11-2025
Valid Till : 25-06-2028
Written Confirmation Number : WC-0023
Address of the Firm : Sy. No’s. 52,53,58,59,61 to 78, 127 & 128,Pydibhimavaram Village & Sy. No’s....
Cefadroxil Monohydrate Ph. Eur
Date of Issue : 07-11-2025
Valid Till : 07-02-2028
Written Confirmation Number : WC-0120
Address of the Firm : UNIT -I, Sy.Nos. 379, 385, 386, 388 to 396, Borpatla Village, Hathnoora Mandal, ...
Cefadroxil Monohydrate BP/Ph. Eur
Date of Issue : 07-07-2025
Valid Till : 31-07-2028
Written Confirmation Number : WC-0048
Address of the Firm : Plot No. — 9, 123, 123/1, 124 & 125, G.I.D.C Estate, Ankleshwar, Dist.- Bharuc...
Date of Issue : 07-07-2025
Valid Till : 31-07-2028
Written Confirmation Number : WC-0048
Address of the Firm : Plot No. — 9, 123, 123/1, 124 & 125, G.I.D.C Estate, Ankleshwar, Dist.- Bharuc...
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PharmaCompass offers a list of Cefadroxil 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 Cefadroxil manufacturer or Cefadroxil supplier for your needs.
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PharmaCompass also assists you with knowing the Cefadroxil API Price utilized in the formulation of products. Cefadroxil API Price is not always fixed or binding as the Cefadroxil Price is obtained through a variety of data sources. The Cefadroxil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Duricef manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duricef, including repackagers and relabelers. The FDA regulates Duricef manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duricef 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 Duricef manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Duricef supplier is an individual or a company that provides Duricef active pharmaceutical ingredient (API) or Duricef finished formulations upon request. The Duricef suppliers may include Duricef API manufacturers, exporters, distributors and traders.
click here to find a list of Duricef suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Duricef written confirmation (Duricef WC) is an official document issued by a regulatory agency to a Duricef manufacturer, verifying that the manufacturing facility of a Duricef active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Duricef APIs or Duricef finished pharmaceutical products to another nation, regulatory agencies frequently require a Duricef WC (written confirmation) as part of the regulatory process.
click here to find a list of Duricef suppliers with Written Confirmation (WC) on PharmaCompass.
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