01 2TITAN LABORATORIES PVT. LTD.@The Andhra Sugars 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...
A Solprin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Solprin, including repackagers and relabelers. The FDA regulates Solprin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Solprin 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 Solprin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Solprin supplier is an individual or a company that provides Solprin active pharmaceutical ingredient (API) or Solprin finished formulations upon request. The Solprin suppliers may include Solprin API manufacturers, exporters, distributors and traders.
click here to find a list of Solprin 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 Solprin Drug Master File in Korea (Solprin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Solprin. The MFDS reviews the Solprin KDMF as part of the drug registration process and uses the information provided in the Solprin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Solprin 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 Solprin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Solprin suppliers with KDMF on PharmaCompass.
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