Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 1CENTRIENT PHARMACEUTICALS NETHERLANDS B.V. Delft NL
02 1ACS DOBFAR S.P.A. Tribiano IT
01 1Cefadroxil monohydrate, Enzymatic process
02 1Cefadroxil monohydrate, Powder, compacted
01 1Italy
02 1Netherlands
01 2Valid
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Cefadroxil Monohydrate, Enzymatic Process
Certificate Number : CEP 2002-156 - Rev 06
Status : Valid
Issue Date : 2024-08-22
Type : Chemical
Substance Number : 813
Cefadroxil Monohydrate, Powder, Compacted
Certificate Number : R1-CEP 1999-174 - Rev 04
Status : Valid
Issue Date : 2023-06-14
Type : Chemical
Substance Number : 813
A Cefadroxil Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefadroxil Monohydrate, including repackagers and relabelers. The FDA regulates Cefadroxil Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefadroxil Monohydrate 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 Cefadroxil Monohydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefadroxil Monohydrate supplier is an individual or a company that provides Cefadroxil Monohydrate active pharmaceutical ingredient (API) or Cefadroxil Monohydrate finished formulations upon request. The Cefadroxil Monohydrate suppliers may include Cefadroxil Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Cefadroxil Monohydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cefadroxil Monohydrate CEP of the European Pharmacopoeia monograph is often referred to as a Cefadroxil Monohydrate Certificate of Suitability (COS). The purpose of a Cefadroxil Monohydrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cefadroxil Monohydrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cefadroxil Monohydrate to their clients by showing that a Cefadroxil Monohydrate CEP has been issued for it. The manufacturer submits a Cefadroxil Monohydrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cefadroxil Monohydrate CEP holder for the record. Additionally, the data presented in the Cefadroxil Monohydrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cefadroxil Monohydrate DMF.
A Cefadroxil Monohydrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cefadroxil Monohydrate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Cefadroxil Monohydrate suppliers with CEP (COS) on PharmaCompass.
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