# Oxybutynin Chloride Extended Release

NDC: 71335-2330
Generic name: Oxybutynin Chloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160927

FDA application: ANDA206121

## 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:"71335-2330"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2330
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2f898b29-46cf-4427-bb64-8c30532222f5