Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1OLPHA AS Olaine LV
01 2Amantadine hydrochloride
01 1Latvia
02 1Spain
01 2Valid
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : R1-CEP 2000-014 - Rev 08
Status : Valid
Issue Date : 2023-05-25
Type : Chemical
Substance Number : 463
Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
Certificate Number : CEP 2017-284 - Rev 03
Status : Valid
Issue Date : 2024-10-28
Type : Chemical
Substance Number : 463
A Amantadine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amantadine, including repackagers and relabelers. The FDA regulates Amantadine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amantadine 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 Amantadine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Amantadine supplier is an individual or a company that provides Amantadine active pharmaceutical ingredient (API) or Amantadine finished formulations upon request. The Amantadine suppliers may include Amantadine API manufacturers, exporters, distributors and traders.
click here to find a list of Amantadine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Amantadine CEP of the European Pharmacopoeia monograph is often referred to as a Amantadine Certificate of Suitability (COS). The purpose of a Amantadine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Amantadine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Amantadine to their clients by showing that a Amantadine CEP has been issued for it. The manufacturer submits a Amantadine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Amantadine CEP holder for the record. Additionally, the data presented in the Amantadine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Amantadine DMF.
A Amantadine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Amantadine 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 Amantadine suppliers with CEP (COS) on PharmaCompass.
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