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PharmaCompass offers a list of Vigabatrin 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 Vigabatrin manufacturer or Vigabatrin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vigabatrin manufacturer or Vigabatrin supplier.
PharmaCompass also assists you with knowing the Vigabatrin API Price utilized in the formulation of products. Vigabatrin API Price is not always fixed or binding as the Vigabatrin Price is obtained through a variety of data sources. The Vigabatrin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vigabatrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vigabatrin, including repackagers and relabelers. The FDA regulates Vigabatrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vigabatrin 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 Vigabatrin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vigabatrin supplier is an individual or a company that provides Vigabatrin active pharmaceutical ingredient (API) or Vigabatrin finished formulations upon request. The Vigabatrin suppliers may include Vigabatrin API manufacturers, exporters, distributors and traders.
click here to find a list of Vigabatrin 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 Vigabatrin Drug Master File in Korea (Vigabatrin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Vigabatrin. The MFDS reviews the Vigabatrin KDMF as part of the drug registration process and uses the information provided in the Vigabatrin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Vigabatrin 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 Vigabatrin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Vigabatrin suppliers with KDMF on PharmaCompass.
We have 2 companies offering Vigabatrin
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