Moehs Group, a reference company in the production of pharmaceutical active ingredients.
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01 1Moehs Iberica S.L. Rubi ES
02 1OLPHA AS Olaine LV
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01 2Amantadine hydrochloride
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01 1Latvia
02 1Spain
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01 2Valid
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amantadine Hydrochloride manufacturer or Amantadine Hydrochloride supplier.
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 Virasol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Virasol, including repackagers and relabelers. The FDA regulates Virasol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Virasol 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 Virasol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Virasol supplier is an individual or a company that provides Virasol active pharmaceutical ingredient (API) or Virasol finished formulations upon request. The Virasol suppliers may include Virasol API manufacturers, exporters, distributors and traders.
click here to find a list of Virasol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Virasol CEP of the European Pharmacopoeia monograph is often referred to as a Virasol Certificate of Suitability (COS). The purpose of a Virasol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Virasol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Virasol to their clients by showing that a Virasol CEP has been issued for it. The manufacturer submits a Virasol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Virasol CEP holder for the record. Additionally, the data presented in the Virasol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Virasol DMF.
A Virasol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Virasol 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 Virasol suppliers with CEP (COS) on PharmaCompass.
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