# Oxybutynin Chloride

NDC: 23155-913
Generic name: Oxybutynin Chloride
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260601

FDA application: ANDA211682

## Active ingredients

- OXYBUTYNIN CHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"23155-913"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-913
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=73d715dc-868d-4194-b668-4c39ababa698