01 1Centaur Pharmaceuticals Private Limited.
02 1Myungin Pharmaceutical Co., Ltd.
01 1Goodwills Co., Ltd.
02 1Myungin Pharmaceutical Co., Ltd.
01 2Triazolam
01 1India
02 1South Korea
Registrant Name : Goodwills Co., Ltd.
Registration Date : 2021-07-27
Registration Number : 20210727-209-J-1079
Manufacturer Name : Centaur Pharmaceuticals Priv...
Manufacturer Address : Plot no. 75, 76 & 76/1 Chikhloli MIDC, Ambernath (West), Thane, Maharashtra, 421501, ...
Registrant Name : Myungin Pharmaceutical Co., Ltd.
Registration Date : 2021-05-17
Registration Number : 20210517-209-J-992
Manufacturer Name : Myungin Pharmaceutical Co., ...
Manufacturer Address : 17 Balan Industrial Complex-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do
A Triazolam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triazolam, including repackagers and relabelers. The FDA regulates Triazolam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triazolam 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 Triazolam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Triazolam supplier is an individual or a company that provides Triazolam active pharmaceutical ingredient (API) or Triazolam finished formulations upon request. The Triazolam suppliers may include Triazolam API manufacturers, exporters, distributors and traders.
click here to find a list of Triazolam 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 Triazolam Drug Master File in Korea (Triazolam KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Triazolam. The MFDS reviews the Triazolam KDMF as part of the drug registration process and uses the information provided in the Triazolam KDMF to evaluate the safety and efficacy of the drug.
After submitting a Triazolam 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 Triazolam API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Triazolam suppliers with KDMF on PharmaCompass.
We have 2 companies offering Triazolam
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