TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

Reset all filters
01 1M/s Teva API India Pvt Ltd
02 1M/s R.L Fine Chem Pvt ltd
03 1M/s RL Fine Chem Pvt Ltd
Reset all filters
01 1Imipramine Hydrochloride BP/USP/Ph. Eur./JP
02 1Imipramine Hydrochloride Ph.Eur./BP/USP
03 1Imipramine Hydrochloride USP/Ph. Eur
Reset all filters
01 1WC-0001
02 1WC-0139
03 1WC-0445
Reset all filters
01 3India
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Imipramine Hydrochloride USP/Ph. Eur
Date of Issue : 2025-06-04
Valid Till : 2028-05-20
Written Confirmation Number : WC-0001
Address of the Firm : Plot No. Q1 to Q4 Industrial Area, Ghirongi, Malanpur, District -Bhind (M.P.), I...
Imipramine Hydrochloride BP/USP/Ph. Eur./JP
Date of Issue : 2025-09-08
Valid Till : 2028-07-07
Written Confirmation Number : WC-0445
Address of the Firm : Plot No. IP No. 27-29, Parts of Sy. Nos. 18, 273, 274 & 313, KIADB Industrial Ar...

Imipramine Hydrochloride Ph.Eur./BP/USP
Date of Issue : 2022-11-02
Valid Till : 2025-07-21
Written Confirmation Number : WC-0139
Address of the Firm : No.15, KHB Industrial Area, Yelahanka, Bangalore- 560064, 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.
A J-002975 written confirmation (J-002975 WC) is an official document issued by a regulatory agency to a J-002975 manufacturer, verifying that the manufacturing facility of a J-002975 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting J-002975 APIs or J-002975 finished pharmaceutical products to another nation, regulatory agencies frequently require a J-002975 WC (written confirmation) as part of the regulatory process.
click here to find a list of J-002975 suppliers with Written Confirmation (WC) on PharmaCompass.
We have 2 companies offering J-002975
Get in contact with the supplier of your choice: