FDA NDC Directory · JSON-LD · Markdown

FLAVOXATE HYDROCHLORIDE

NDC 0574-0115 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPadagis US LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076831
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLAVOXATE HYDROCHLORIDE (100 mg/1)
Marketing started20041222
Marketing ended20261231
Package count1

External sources

Source: openFDA. Public-domain (CC0).