# Oxybutynin Chloride

NDC: 60687-899
Generic name: Oxybutynin Chloride
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260416

FDA application: ANDA208165

## Active ingredients

- OXYBUTYNIN CHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-899"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-899
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4574b227-9726-4798-bac2-83bfb9616f09