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Imipramine Hydrochloride

NDC 82804-957 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA040751
Dosage form / routeTABLET · ORAL
Active ingredientsIMIPRAMINE HYDROCHLORIDE (25 mg/1)
Marketing started20200801
Package count7

External sources

Source: openFDA. Public-domain (CC0).