01 1Dongying Tiandong Pharmaceutical Co., Ltd. Dongying City CN
02 1GLAND PHARMA LIMITED Hyderabad IN
03 1Opocrin SpA - CORLO PLANT Corlo Di Formigine IT
01 3Enoxaparin sodium
01 1China
02 1India
03 1Italy
01 2Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2005-258 - Rev 05
Status : Valid
Issue Date : 2021-07-23
Type : Chemical
Substance Number : 1097
Certificate Number : CEP 2003-266 - Rev 04
Status : Valid
Issue Date : 2024-11-04
Type : Chemical
Substance Number : 1097
Certificate Number : R1-CEP 2004-014 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2010-08-05
Type : Chemical
Substance Number : 1097
A Enoxaparin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Enoxaparin Sodium, including repackagers and relabelers. The FDA regulates Enoxaparin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Enoxaparin Sodium 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 Enoxaparin Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Enoxaparin Sodium supplier is an individual or a company that provides Enoxaparin Sodium active pharmaceutical ingredient (API) or Enoxaparin Sodium finished formulations upon request. The Enoxaparin Sodium suppliers may include Enoxaparin Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Enoxaparin Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Enoxaparin Sodium CEP of the European Pharmacopoeia monograph is often referred to as a Enoxaparin Sodium Certificate of Suitability (COS). The purpose of a Enoxaparin Sodium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Enoxaparin Sodium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Enoxaparin Sodium to their clients by showing that a Enoxaparin Sodium CEP has been issued for it. The manufacturer submits a Enoxaparin Sodium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Enoxaparin Sodium CEP holder for the record. Additionally, the data presented in the Enoxaparin Sodium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Enoxaparin Sodium DMF.
A Enoxaparin Sodium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Enoxaparin Sodium 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 Enoxaparin Sodium suppliers with CEP (COS) on PharmaCompass.
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