01 1Lundbeck Pharmaceuticals Italy SPA
01 1Samoh Pharmaceutical Co., Ltd.
01 1Clomipramine hydrochloride
01 1Denmark
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2022-01-21
Registration Number : 20220121-211-J-1168
Manufacturer Name : Lundbeck Pharmaceuticals Ita...
Manufacturer Address : Viale dell'Industria 54 - 35129, Padova (PD) Italy
A Clomipramine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clomipramine Hydrochloride, including repackagers and relabelers. The FDA regulates Clomipramine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clomipramine 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 Clomipramine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clomipramine Hydrochloride supplier is an individual or a company that provides Clomipramine Hydrochloride active pharmaceutical ingredient (API) or Clomipramine Hydrochloride finished formulations upon request. The Clomipramine Hydrochloride suppliers may include Clomipramine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Clomipramine 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 Clomipramine Hydrochloride Drug Master File in Korea (Clomipramine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Clomipramine Hydrochloride. The MFDS reviews the Clomipramine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Clomipramine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Clomipramine 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 Clomipramine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Clomipramine Hydrochloride suppliers with KDMF on PharmaCompass.
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