FDA NDC Directory · JSON-LD · Markdown

Oxybutynin Chloride

NDC 67046-1381 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208165
Dosage form / routeTABLET · ORAL
Active ingredientsOXYBUTYNIN CHLORIDE (5 mg/1)
Marketing started20260706
Marketing ended20270831
Package count1

External sources

Source: openFDA. Public-domain (CC0).