01 1TITAN LABORATORIES PVT. LTD.@The Andhra Sugars Ltd.
02 1TITAN LABORATORIES PVT. LTD.@The Andhra Sugars Ltd.@Alta Laboratories Ltd
01 1Bansen Co., Ltd.
02 1Hanmi Pharmaceutical Co., Ltd.
01 2Aspirin enteric pellets
01 2India
Registrant Name : Hanmi Pharmaceutical Co., Ltd.
Registration Date : 2023-10-04
Registration Number : 20230809-211-J-1538(1)
Manufacturer Name : TITAN LABORATORIES PVT. LTD....
Manufacturer Address : E27/1 & E27/2, MIDC Mahad, Village - JITE, Dist-Raigad, Pin-402309 Maharashtra State,...
Registrant Name : Bansen Co., Ltd.
Registration Date : 2023-08-09
Registration Number : 20230809-211-J-1538
Manufacturer Name : TITAN LABORATORIES PVT. LTD....
Manufacturer Address : Plot No. E-27/1 & E-27/2, MIDC Mahad, Village - JITE, Raigad 402309 Maharashtra State...
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A component of St. Joseph Cold Tablets manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of component of St. Joseph Cold Tablets, including repackagers and relabelers. The FDA regulates component of St. Joseph Cold Tablets manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. component of St. Joseph Cold Tablets 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 component of St. Joseph Cold Tablets supplier is an individual or a company that provides component of St. Joseph Cold Tablets active pharmaceutical ingredient (API) or component of St. Joseph Cold Tablets finished formulations upon request. The component of St. Joseph Cold Tablets suppliers may include component of St. Joseph Cold Tablets 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 component of St. Joseph Cold Tablets Drug Master File in Korea (component of St. Joseph Cold Tablets KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of component of St. Joseph Cold Tablets. The MFDS reviews the component of St. Joseph Cold Tablets KDMF as part of the drug registration process and uses the information provided in the component of St. Joseph Cold Tablets KDMF to evaluate the safety and efficacy of the drug.
After submitting a component of St. Joseph Cold Tablets 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 component of St. Joseph Cold Tablets API can apply through the Korea Drug Master File (KDMF).
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