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oxybutynin chloride

NDC 71205-667 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA207138
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsOXYBUTYNIN CHLORIDE (10 mg/1)
Marketing started20161220
Package count3

External sources

Source: openFDA. Public-domain (CC0).