01 1Excella GmbH & Co. KG
02 1Solara Active Pharma Sciences Limited
01 1Masung LS Co., Ltd.
02 1Samoh Pharmaceutical Co., Ltd.
01 2Buspirone hydrochloride
01 1India
02 1Luxembourg
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2018-10-11
Registration Number : 20181011-209-J-136
Manufacturer Name : Excella GmbH & Co. KG
Manufacturer Address : Nurnberger Str. 12, 90537 Feucht, Germany
Registrant Name : Masung LS Co., Ltd.
Registration Date : 2021-12-28
Registration Number : 20211228-209-J-1093
Manufacturer Name : Solara Active Pharma Science...
Manufacturer Address : 120 A&B, 120P & 121, Industrial Area Baikampady New Mangalore – 575 011, Karnataka,...
A Buspirone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buspirone Hydrochloride, including repackagers and relabelers. The FDA regulates Buspirone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buspirone 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 Buspirone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Buspirone Hydrochloride supplier is an individual or a company that provides Buspirone Hydrochloride active pharmaceutical ingredient (API) or Buspirone Hydrochloride finished formulations upon request. The Buspirone Hydrochloride suppliers may include Buspirone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Buspirone Hydrochloride 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 Buspirone Hydrochloride Drug Master File in Korea (Buspirone Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Buspirone Hydrochloride. The MFDS reviews the Buspirone Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Buspirone Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Buspirone 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 Buspirone Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Buspirone Hydrochloride suppliers with KDMF on PharmaCompass.
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