FDA NDC Directory · JSON-LD · Markdown

OXAPROZIN

NDC 62135-176 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerChartwell RX, LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA075987
Dosage form / routeTABLET · ORAL
Active ingredientsOXAPROZIN (600 mg/1)
Marketing started20040902
Package count2

External sources

Source: openFDA. Public-domain (CC0).