# Oxybutynin Chloride

NDC: 50111-456
Generic name: Oxybutynin Chloride
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19900930

FDA application: ANDA071655

## Active ingredients

- OXYBUTYNIN CHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50111-456"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50111-456
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb7aba8d-6913-4f57-8eb4-c6d6ff0b2a29