FDA NDC Directory · JSON-LD · Markdown

Diflunisal

NDC 0093-9222 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA073673
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDIFLUNISAL (500 mg/1)
Marketing started20210630
Package count3

External sources

Source: openFDA. Public-domain (CC0).