API Suppliers
US DMFs Filed
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EU WC
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U.S. Medicaid
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PharmaCompass offers a list of Ramipril 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 Ramipril manufacturer or Ramipril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ramipril manufacturer or Ramipril supplier.
PharmaCompass also assists you with knowing the Ramipril API Price utilized in the formulation of products. Ramipril API Price is not always fixed or binding as the Ramipril Price is obtained through a variety of data sources. The Ramipril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ramipril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ramipril, including repackagers and relabelers. The FDA regulates Ramipril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ramipril 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 Ramipril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ramipril supplier is an individual or a company that provides Ramipril active pharmaceutical ingredient (API) or Ramipril finished formulations upon request. The Ramipril suppliers may include Ramipril API manufacturers, exporters, distributors and traders.
click here to find a list of Ramipril 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 Ramipril Drug Master File in Korea (Ramipril KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ramipril. The MFDS reviews the Ramipril KDMF as part of the drug registration process and uses the information provided in the Ramipril KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ramipril 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 Ramipril API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ramipril suppliers with KDMF on PharmaCompass.