FDA NDC Directory · JSON-LD · Markdown

Oxybutynin Chloride

NDC 68788-8141 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209335
Dosage form / routeTABLET · ORAL
Active ingredientsOXYBUTYNIN CHLORIDE (5 mg/1)
Marketing started20220211
Package count1

External sources

Source: openFDA. Public-domain (CC0).