01 1PCAS
01 1Samoh Pharmaceutical Co., Ltd.
01 1Oxybutynin hydrochloride
01 1France
Registrant Name : Samoh 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
48
PharmaCompass offers a list of Oxybutynin Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Oxybutynin Hydrochloride manufacturer or Oxybutynin Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Oxybutynin Hydrochloride API Price utilized in the formulation of products. Oxybutynin Hydrochloride API Price is not always fixed or binding as the Oxybutynin Hydrochloride Price is obtained through a variety of data sources. The Oxybutynin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KS-1377 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KS-1377, including repackagers and relabelers. The FDA regulates KS-1377 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KS-1377 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 KS-1377 supplier is an individual or a company that provides KS-1377 active pharmaceutical ingredient (API) or KS-1377 finished formulations upon request. The KS-1377 suppliers may include KS-1377 API manufacturers, exporters, distributors and traders.
click here to find a list of KS-1377 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 KS-1377 Drug Master File in Korea (KS-1377 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of KS-1377. The MFDS reviews the KS-1377 KDMF as part of the drug registration process and uses the information provided in the KS-1377 KDMF to evaluate the safety and efficacy of the drug.
After submitting a KS-1377 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 KS-1377 API can apply through the Korea Drug Master File (KDMF).
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