# Oxybutynin Chloride

NDC: 67046-1381
Generic name: Oxybutynin Chloride
Labeler / Manufacturer: Coupler LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260706
Marketing ended: 20270831
FDA application: ANDA208165

## Active ingredients

- OXYBUTYNIN CHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67046-1381"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67046-1381
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=55f618d1-4463-3200-e063-6394a90a89a8