FDA NDC Directory · JSON-LD · Markdown

OXYTROL

NDC 0023-6153 · HUMAN PRESCRIPTION DRUG · PATCH

Generic nameOxybutynin
Labeler / ManufacturerAllergan, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA021351
Dosage form / routePATCH · TRANSDERMAL
Active ingredientsOXYBUTYNIN (3.9 mg/d)
Marketing started20030226
Package count1

External sources

Source: openFDA. Public-domain (CC0).