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 1Sam-O 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 : Sam-O 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
40
PharmaCompass offers a list of Imipramine 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 Imipramine Hydrochloride manufacturer or Imipramine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Imipramine Hydrochloride manufacturer or Imipramine Hydrochloride supplier.
A J-002975 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of J-002975, including repackagers and relabelers. The FDA regulates J-002975 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. J-002975 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 J-002975 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A J-002975 supplier is an individual or a company that provides J-002975 active pharmaceutical ingredient (API) or J-002975 finished formulations upon request. The J-002975 suppliers may include J-002975 API manufacturers, exporters, distributors and traders.
click here to find a list of J-002975 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 J-002975 Drug Master File in Korea (J-002975 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of J-002975. The MFDS reviews the J-002975 KDMF as part of the drug registration process and uses the information provided in the J-002975 KDMF to evaluate the safety and efficacy of the drug.
After submitting a J-002975 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 J-002975 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of J-002975 suppliers with KDMF on PharmaCompass.
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