01 1Erregierre SpA
01 1Sam-O Pharmaceutical Co., Ltd.
01 1Urapidil
01 1Italy
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2020-06-24
Registration Number : 20200624-211-J-564
Manufacturer Name : Erregierre SpA
Manufacturer Address : Via Francesco. Baracca, 19-24060 SAN PAOLO D'ARGON (BG), Italy
20
PharmaCompass offers a list of Urapidil 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 Urapidil Hydrochloride manufacturer or Urapidil Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Urapidil Hydrochloride manufacturer or Urapidil Hydrochloride supplier.
A Urapidil Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urapidil Hydrochloride, including repackagers and relabelers. The FDA regulates Urapidil Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urapidil 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.
click here to find a list of Urapidil Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Urapidil Hydrochloride supplier is an individual or a company that provides Urapidil Hydrochloride active pharmaceutical ingredient (API) or Urapidil Hydrochloride finished formulations upon request. The Urapidil Hydrochloride suppliers may include Urapidil Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Urapidil Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Urapidil Hydrochloride Drug Master File in Korea (Urapidil Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Urapidil Hydrochloride. The MFDS reviews the Urapidil Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Urapidil Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Urapidil 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 Urapidil Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Urapidil Hydrochloride suppliers with KDMF on PharmaCompass.
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