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
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PharmaCompass offers a list of Amantadine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Amantadine Hydrochloride manufacturer or Amantadine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Amantadine Hydrochloride API Price utilized in the formulation of products. Amantadine Hydrochloride API Price is not always fixed or binding as the Amantadine Hydrochloride Price is obtained through a variety of data sources. The Amantadine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Symadine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Symadine, including repackagers and relabelers. The FDA regulates Symadine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Symadine 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 Symadine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Symadine supplier is an individual or a company that provides Symadine active pharmaceutical ingredient (API) or Symadine finished formulations upon request. The Symadine suppliers may include Symadine API manufacturers, exporters, distributors and traders.
click here to find a list of Symadine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Symadine CEP of the European Pharmacopoeia monograph is often referred to as a Symadine Certificate of Suitability (COS). The purpose of a Symadine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Symadine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Symadine to their clients by showing that a Symadine CEP has been issued for it. The manufacturer submits a Symadine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Symadine CEP holder for the record. Additionally, the data presented in the Symadine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Symadine DMF.
A Symadine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Symadine 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 Symadine suppliers with CEP (COS) on PharmaCompass.
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