FDA NDC Directory · JSON-LD · Markdown

OXYBUTYNIN CHLORIDE

NDC 72189-130 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / Manufacturerdirect rx
Marketing categoryAbbreviated NDA (generic) · App ANDA071655
Dosage form / routeTABLET · ORAL
Active ingredientsOXYBUTYNIN CHLORIDE (5 mg/1)
Marketing started20201111
Package count1

External sources

Source: openFDA. Public-domain (CC0).