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 2North China Pharmaceutical Group Semisyntech Co., Ltd. Shijiazhuang CN
03 1SANDOZ GMBH Kundl AT
01 1Benzylpenicillin (procaine) monohydrate
02 1Benzylpenicillin (procaine) monohydrate, Sterile
03 1Benzylpenicillin (procaine) monohydrate, Sterile, lecithin coated (1%)
04 1Benzylpenicillin (procaine) monohydrate, Sterile, microfine
01 2China
02 1Germany
03 1Netherlands
01 2Valid
02 2Withdrawn by EDQM Failure to CEP procedure
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.
Benzylpenicillin (procaine) Monohydrate
Certificate Number : R0-CEP 2020-147 - Rev 00
Status : Valid
Issue Date : 2022-08-31
Type : Chemical
Substance Number : 115
Benzylpenicillin (procaine) Monohydrate, Sterile
Certificate Number : R1-CEP 2004-001 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2014-07-11
Type : Chemical
Substance Number : 115
Benzylpenicillin (procaine) Monohydrate, Sterile...
Certificate Number : R1-CEP 2004-017 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2014-07-11
Type : Chemical
Substance Number : 115
Benzylpenicillin (procaine) Monohydrate, Sterile...
Certificate Number : R2-CEP 1995-003 - Rev 04
Status : Valid
Issue Date : 2019-12-05
Type : Chemical
Substance Number : 115
81
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A Despacilina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Despacilina, including repackagers and relabelers. The FDA regulates Despacilina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Despacilina 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 Despacilina supplier is an individual or a company that provides Despacilina active pharmaceutical ingredient (API) or Despacilina finished formulations upon request. The Despacilina suppliers may include Despacilina API manufacturers, exporters, distributors and traders.
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A Despacilina CEP of the European Pharmacopoeia monograph is often referred to as a Despacilina Certificate of Suitability (COS). The purpose of a Despacilina CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Despacilina EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Despacilina to their clients by showing that a Despacilina CEP has been issued for it. The manufacturer submits a Despacilina CEP (COS) as part of the market authorization procedure, and it takes on the role of a Despacilina CEP holder for the record. Additionally, the data presented in the Despacilina CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Despacilina DMF.
A Despacilina CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Despacilina 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 Despacilina suppliers with CEP (COS) on PharmaCompass.
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