01 1Hwail Pharmaceutical Co., Ltd.
01 1Hwail Pharmaceutical Co., Ltd.
01 1Clenbuterol hydrochlorideClenbuterol hydrochloride
01 1South Korea
Clenbuterol hydrochlorideClenbuterol hydrochloride
Registrant Name : Hwail Pharmaceutical Co., Ltd.
Registration Date : 2021-11-03
Registration Number : 20211103-211-J-1136
Manufacturer Name : Hwail Pharmaceutical Co., Lt...
Manufacturer Address : 57, Yakjakgongdan 3-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do
A Clenbuterol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clenbuterol Hydrochloride, including repackagers and relabelers. The FDA regulates Clenbuterol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clenbuterol Hydrochloride 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 Clenbuterol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clenbuterol Hydrochloride supplier is an individual or a company that provides Clenbuterol Hydrochloride active pharmaceutical ingredient (API) or Clenbuterol Hydrochloride finished formulations upon request. The Clenbuterol Hydrochloride suppliers may include Clenbuterol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Clenbuterol Hydrochloride 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 Clenbuterol Hydrochloride Drug Master File in Korea (Clenbuterol Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Clenbuterol Hydrochloride. The MFDS reviews the Clenbuterol Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Clenbuterol Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Clenbuterol Hydrochloride 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 Clenbuterol Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Clenbuterol Hydrochloride suppliers with KDMF on PharmaCompass.
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