# OXYBUTYNIN CHLORIDE

NDC: 72189-131
Generic name: OXYBUTYNIN CHLORIDE
Labeler / Manufacturer: direct rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20201111

FDA application: ANDA207138

## 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:"72189-131"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-131
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b3d6d2a8-97c4-5bad-e053-2a95a90a155d