01 1Biotika A.S. Slovenska Lupca SK
02 1DSM Anti-Infectives B.V. Delft NL
03 1North China Pharmaceutical Co., LTD. Shijiazhuang CN
04 1SANDOZ GMBH Kundl AT
01 3Phenoxymethylpenicillin potassium
02 1Phenoxymethylpenicillin potassium, Material Code Numbers 450401, 450402 and 451786
01 1China
02 1Germany
03 1Netherlands
04 1Slovakia
01 2Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 1Withdrawn by Holder
Phenoxymethylpenicillin Potassium
Certificate Number : R1-CEP 1997-043 - Rev 02
Status : Valid
Issue Date : 2008-02-08
Type : Chemical
Substance Number : 149
Phenoxymethylpenicillin Potassium
Certificate Number : R0-CEP 2006-019 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2008-11-26
Type : Chemical
Substance Number : 149
Phenoxymethylpenicillin Potassium, Material Code...
Certificate Number : R2-CEP 1994-012 - Rev 06
Status : Valid
Issue Date : 2017-05-15
Type : Chemical
Substance Number : 149
Phenoxymethylpenicillin Potassium
Certificate Number : R1-CEP 1994-017 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2002-04-16
Type : Chemical
Substance Number : 149
15
PharmaCompass offers a list of Penicillin V Potassium 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 Penicillin V Potassium manufacturer or Penicillin V Potassium supplier for your needs.
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A Megacillin oral manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Megacillin oral, including repackagers and relabelers. The FDA regulates Megacillin oral manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Megacillin oral 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 Megacillin oral supplier is an individual or a company that provides Megacillin oral active pharmaceutical ingredient (API) or Megacillin oral finished formulations upon request. The Megacillin oral suppliers may include Megacillin oral API manufacturers, exporters, distributors and traders.
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A Megacillin oral CEP of the European Pharmacopoeia monograph is often referred to as a Megacillin oral Certificate of Suitability (COS). The purpose of a Megacillin oral CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Megacillin oral EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Megacillin oral to their clients by showing that a Megacillin oral CEP has been issued for it. The manufacturer submits a Megacillin oral CEP (COS) as part of the market authorization procedure, and it takes on the role of a Megacillin oral CEP holder for the record. Additionally, the data presented in the Megacillin oral CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Megacillin oral DMF.
A Megacillin oral CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Megacillin oral CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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