FDA NDC Directory · JSON-LD · Markdown

Amoxapine

NDC 62135-702 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerChartwell RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA072879
Dosage form / routeTABLET · ORAL
Active ingredientsAMOXAPINE (100 mg/1)
Marketing started19910628
Package count1

External sources

Source: openFDA. Public-domain (CC0).