01 1ScinoPharm Taiwan, Ltd.
01 1Korea Pfizer Pharmaceutical Co., Ltd.
01 1Exemestane
01 1Taiwan
Registrant Name : Korea Pfizer Pharmaceutical Co., Ltd.
Registration Date : 2025-10-29
Registration Number : Su87-44-ND
Manufacturer Name : ScinoPharm Taiwan, Ltd.
Manufacturer Address : No. 1, Nan-ke 8th Road, Shan-Hua, Tainan 741014, Taiwan
98
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A 6-methylideneandrosta-1,4-diene-3,17-dione manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 6-methylideneandrosta-1,4-diene-3,17-dione, including repackagers and relabelers. The FDA regulates 6-methylideneandrosta-1,4-diene-3,17-dione manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 6-methylideneandrosta-1,4-diene-3,17-dione 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 6-methylideneandrosta-1,4-diene-3,17-dione supplier is an individual or a company that provides 6-methylideneandrosta-1,4-diene-3,17-dione active pharmaceutical ingredient (API) or 6-methylideneandrosta-1,4-diene-3,17-dione finished formulations upon request. The 6-methylideneandrosta-1,4-diene-3,17-dione suppliers may include 6-methylideneandrosta-1,4-diene-3,17-dione 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 6-methylideneandrosta-1,4-diene-3,17-dione Drug Master File in Korea (6-methylideneandrosta-1,4-diene-3,17-dione KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 6-methylideneandrosta-1,4-diene-3,17-dione. The MFDS reviews the 6-methylideneandrosta-1,4-diene-3,17-dione KDMF as part of the drug registration process and uses the information provided in the 6-methylideneandrosta-1,4-diene-3,17-dione KDMF to evaluate the safety and efficacy of the drug.
After submitting a 6-methylideneandrosta-1,4-diene-3,17-dione 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 6-methylideneandrosta-1,4-diene-3,17-dione API can apply through the Korea Drug Master File (KDMF).
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