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PharmaCompass offers a list of Memantine 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 Memantine Hydrochloride manufacturer or Memantine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Memantine Hydrochloride manufacturer or Memantine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Memantine Hydrochloride API Price utilized in the formulation of products. Memantine Hydrochloride API Price is not always fixed or binding as the Memantine Hydrochloride Price is obtained through a variety of data sources. The Memantine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Memantine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Memantine, including repackagers and relabelers. The FDA regulates Memantine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Memantine 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 Memantine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Memantine supplier is an individual or a company that provides Memantine active pharmaceutical ingredient (API) or Memantine finished formulations upon request. The Memantine suppliers may include Memantine API manufacturers, exporters, distributors and traders.
click here to find a list of Memantine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Memantine Drug Master File in Korea (Memantine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Memantine. The MFDS reviews the Memantine KDMF as part of the drug registration process and uses the information provided in the Memantine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Memantine KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Memantine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Memantine suppliers with KDMF on PharmaCompass.
We have 10 companies offering Memantine
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