01 1PCAS
01 1Sam-O Pharmaceutical Co., Ltd.
01 1Oxybutinine hydrochloride
01 1France
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2022-01-13
Registration Number : 20220113-209-J-1211
Manufacturer Name : PCAS
Manufacturer Address : 19 route de Meulan, LIMAY, 78520, France
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PharmaCompass offers a list of Oxybutynin Hydrochloride 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 Oxybutynin Hydrochloride manufacturer or Oxybutynin Hydrochloride supplier for your needs.
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A Oxibutinina hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxibutinina hydrochloride, including repackagers and relabelers. The FDA regulates Oxibutinina hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxibutinina 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.
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A Oxibutinina hydrochloride supplier is an individual or a company that provides Oxibutinina hydrochloride active pharmaceutical ingredient (API) or Oxibutinina hydrochloride finished formulations upon request. The Oxibutinina hydrochloride suppliers may include Oxibutinina hydrochloride 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 Oxibutinina hydrochloride Drug Master File in Korea (Oxibutinina hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Oxibutinina hydrochloride. The MFDS reviews the Oxibutinina hydrochloride KDMF as part of the drug registration process and uses the information provided in the Oxibutinina hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Oxibutinina 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 Oxibutinina hydrochloride API can apply through the Korea Drug Master File (KDMF).
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