01 1Fersinsa GB S.A. De C.V. Ramos Arizpe MX
02 1PARABOLIC DRUGS LIMITED Panchkula District IN
03 1Sandoz Industrial Products S.A. Les Franqueses Del Vallès ES
01 1Ampicillin
02 1Ampicillin, Mexico
03 1Ampicillin, Powder, compacted
01 1Germany
02 1India
03 1Netherlands
01 2Valid
02 1Withdrawn by EDQM Failure to CEP procedure
Certificate Number : R0-CEP 2011-090 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2013-03-07
Type : Chemical
Substance Number : 167
Certificate Number : R2-CEP 1995-031 - Rev 05
Status : Valid
Issue Date : 2022-02-21
Type : Chemical
Substance Number : 167
Certificate Number : R1-CEP 1999-188 - Rev 03
Status : Valid
Issue Date : 2018-01-15
Type : Chemical
Substance Number : 167
A Penbritin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Penbritin, including repackagers and relabelers. The FDA regulates Penbritin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Penbritin 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 Penbritin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Penbritin supplier is an individual or a company that provides Penbritin active pharmaceutical ingredient (API) or Penbritin finished formulations upon request. The Penbritin suppliers may include Penbritin API manufacturers, exporters, distributors and traders.
click here to find a list of Penbritin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Penbritin CEP of the European Pharmacopoeia monograph is often referred to as a Penbritin Certificate of Suitability (COS). The purpose of a Penbritin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Penbritin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Penbritin to their clients by showing that a Penbritin CEP has been issued for it. The manufacturer submits a Penbritin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Penbritin CEP holder for the record. Additionally, the data presented in the Penbritin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Penbritin DMF.
A Penbritin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Penbritin 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 Penbritin suppliers with CEP (COS) on PharmaCompass.
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