FDA NDC Directory · JSON-LD · Markdown

Amoxapine

NDC 0591-5715 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA072691
Dosage form / routeTABLET · ORAL
Active ingredientsAMOXAPINE (100 mg/1)
Marketing started19920828
Package count1

External sources

Source: openFDA. Public-domain (CC0).