01 1Wuhan Wuyao Pharmaceutical Co.,Ltd.
01 1Ace Biopharm Co., Ltd.
01 1Ethambutol hydrochloride
01 1China
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2019-04-04
Registration Number : 20190404-211-J-331
Manufacturer Name : Wuhan Wuyao Pharmaceutical C...
Manufacturer Address : No. 18, Wangfen Road, Fuchi Town, Yangxin County, huangshi City Hubei Province, China
96
PharmaCompass offers a list of Ethambutol Dihydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Ethambutol Dihydrochloride manufacturer or Ethambutol Dihydrochloride supplier for your needs.
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A C10H24N2O2.2HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C10H24N2O2.2HCl, including repackagers and relabelers. The FDA regulates C10H24N2O2.2HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C10H24N2O2.2HCl 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 C10H24N2O2.2HCl supplier is an individual or a company that provides C10H24N2O2.2HCl active pharmaceutical ingredient (API) or C10H24N2O2.2HCl finished formulations upon request. The C10H24N2O2.2HCl suppliers may include C10H24N2O2.2HCl 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 C10H24N2O2.2HCl Drug Master File in Korea (C10H24N2O2.2HCl KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of C10H24N2O2.2HCl. The MFDS reviews the C10H24N2O2.2HCl KDMF as part of the drug registration process and uses the information provided in the C10H24N2O2.2HCl KDMF to evaluate the safety and efficacy of the drug.
After submitting a C10H24N2O2.2HCl 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 C10H24N2O2.2HCl API can apply through the Korea Drug Master File (KDMF).
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