FDA NDC Directory · JSON-LD · Markdown

Oxybutynin Chloride

NDC 52817-260 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameoxybutynin chloride
Labeler / ManufacturerTruPharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210125
Dosage form / routeTABLET · ORAL
Active ingredientsOXYBUTYNIN CHLORIDE (5 mg/1)
Marketing started20190101
Package count2

External sources

Source: openFDA. Public-domain (CC0).