TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1Teva API (India) Private Limited
01 1Samoh Pharmaceutical Co., Ltd.
01 1Imipramine hydrochloride
01 1Israel
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2021-05-04
Registration Number : 20210504-209-J-976
Manufacturer Name : Teva API (India) Private Lim...
Manufacturer Address : Q1 to Q4 Industrial Area, Ghirongi Malanpur Bhind, Madhya Pradesh State, India
A Imipramine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Imipramine Hydrochloride, including repackagers and relabelers. The FDA regulates Imipramine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Imipramine 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 Imipramine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Imipramine Hydrochloride supplier is an individual or a company that provides Imipramine Hydrochloride active pharmaceutical ingredient (API) or Imipramine Hydrochloride finished formulations upon request. The Imipramine Hydrochloride suppliers may include Imipramine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Imipramine 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 Imipramine Hydrochloride Drug Master File in Korea (Imipramine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Imipramine Hydrochloride. The MFDS reviews the Imipramine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Imipramine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Imipramine 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 Imipramine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Imipramine Hydrochloride suppliers with KDMF on PharmaCompass.
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