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Imipramine Hydrochloride

NDC 70868-810 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerKey Therapeutics
Marketing categoryAbbreviated NDA (generic) · App ANDA040751
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIMIPRAMINE HYDROCHLORIDE (25 mg/1)
Marketing started20220718
Package count1

External sources

Source: openFDA. Public-domain (CC0).