01 1Apitoria Pharma Private Limited, Unit-I@Aurobindo Pharma Limited
02 1Assia Chemical Industries Ltd. (Teva Tech site)
01 1JDW Pharmaceutical Co., Ltd.
02 1Seongi Bio Co., Ltd.
01 2Modafinil
01 1India
02 1Israel
Registrant Name : JDW Pharmaceutical Co., Ltd.
Registration Date : 2023-05-11
Registration Number : 20230511-209-J-1490
Manufacturer Name : Assia Chemical Industries Lt...
Manufacturer Address : Neot-Hovav Eco-Ind. Park, Emek Sara, P.OB. 2049, Be'er Sheva, 8412316, Israel
Registrant Name : Seongi Bio Co., Ltd.
Registration Date : 2020-02-27
Registration Number : 20200227-209-J-317
Manufacturer Name : Apitoria Pharma Private Limi...
Manufacturer Address : Sy.No. 379, 385, 386, 388 - 396, Borpatla Village, Hatnoora Mandal, Sangareddy Distri...
A Provigil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Provigil, including repackagers and relabelers. The FDA regulates Provigil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Provigil 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 Provigil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Provigil supplier is an individual or a company that provides Provigil active pharmaceutical ingredient (API) or Provigil finished formulations upon request. The Provigil suppliers may include Provigil API manufacturers, exporters, distributors and traders.
click here to find a list of Provigil 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 Provigil Drug Master File in Korea (Provigil KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Provigil. The MFDS reviews the Provigil KDMF as part of the drug registration process and uses the information provided in the Provigil KDMF to evaluate the safety and efficacy of the drug.
After submitting a Provigil 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 Provigil API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Provigil suppliers with KDMF on PharmaCompass.
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