01 1FIS Fabbrica Italiana Sintetici SpA
02 1Myungin Pharmaceutical Co., Ltd.
01 1Myungin Pharmaceutical Co., Ltd.
02 1Samoh Pharmaceutical Co., Ltd.
01 2Bromazepam
01 1Italy
02 1South Korea
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2021-04-16
Registration Number : 20210416-209-J-848
Manufacturer Name : FIS Fabbrica Italiana Sintet...
Manufacturer Address : Viale Milano, 26-36075 MONTECCHIO MAGGIORE (VI), Italy
Registrant Name : Myungin Pharmaceutical Co., Ltd.
Registration Date : 2025-09-26
Registration Number : 20250926-209-J-2029
Manufacturer Name : Myungin Pharmaceutical Co., ...
Manufacturer Address : 17 Balan Industrial Complex-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do
25
PharmaCompass offers a list of Bromazepam 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 Bromazepam manufacturer or Bromazepam supplier for your needs.
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A Lexotan, Lexotanil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lexotan, Lexotanil, including repackagers and relabelers. The FDA regulates Lexotan, Lexotanil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lexotan, Lexotanil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Lexotan, Lexotanil supplier is an individual or a company that provides Lexotan, Lexotanil active pharmaceutical ingredient (API) or Lexotan, Lexotanil finished formulations upon request. The Lexotan, Lexotanil suppliers may include Lexotan, Lexotanil API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Lexotan, Lexotanil Drug Master File in Korea (Lexotan, Lexotanil KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Lexotan, Lexotanil. The MFDS reviews the Lexotan, Lexotanil KDMF as part of the drug registration process and uses the information provided in the Lexotan, Lexotanil KDMF to evaluate the safety and efficacy of the drug.
After submitting a Lexotan, Lexotanil 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 Lexotan, Lexotanil API can apply through the Korea Drug Master File (KDMF).
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