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Oxybutynin Chloride Extended Release

NDC 68084-480 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic nameOxybutynin Chloride
Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA078503
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsOXYBUTYNIN CHLORIDE (5 mg/1)
Marketing started20120113
Package count2

External sources

Source: openFDA. Public-domain (CC0).