Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
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01 1CENTRIENT PHARMACEUTICALS NETHERLANDS B.V. Delft NL
02 2North China Pharmaceutical Group Semisyntech Co., Ltd. Shijiazhuang CN
03 1SANDOZ GMBH Kundl AT
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01 1Benzylpenicillin (procaine) monohydrate
02 1Benzylpenicillin (procaine) monohydrate, Sterile
03 1Benzylpenicillin (procaine) monohydrate, Sterile, lecithin coated (1%)
04 1Benzylpenicillin (procaine) monohydrate, Sterile, microfine
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01 2China
02 1Germany
03 1Netherlands
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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Status : Withdrawn by EDQM Failure to CEP pro...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Status : Withdrawn by EDQM Failure to CEP pro...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 NOVOCAINE PENICILLIN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NOVOCAINE PENICILLIN, including repackagers and relabelers. The FDA regulates NOVOCAINE PENICILLIN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NOVOCAINE PENICILLIN 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 NOVOCAINE PENICILLIN supplier is an individual or a company that provides NOVOCAINE PENICILLIN active pharmaceutical ingredient (API) or NOVOCAINE PENICILLIN finished formulations upon request. The NOVOCAINE PENICILLIN suppliers may include NOVOCAINE PENICILLIN API manufacturers, exporters, distributors and traders.
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A NOVOCAINE PENICILLIN CEP of the European Pharmacopoeia monograph is often referred to as a NOVOCAINE PENICILLIN Certificate of Suitability (COS). The purpose of a NOVOCAINE PENICILLIN CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of NOVOCAINE PENICILLIN EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of NOVOCAINE PENICILLIN to their clients by showing that a NOVOCAINE PENICILLIN CEP has been issued for it. The manufacturer submits a NOVOCAINE PENICILLIN CEP (COS) as part of the market authorization procedure, and it takes on the role of a NOVOCAINE PENICILLIN CEP holder for the record. Additionally, the data presented in the NOVOCAINE PENICILLIN CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the NOVOCAINE PENICILLIN DMF.
A NOVOCAINE PENICILLIN CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. NOVOCAINE PENICILLIN 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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