# Oxybutynin Chloride

NDC: 52817-260
Generic name: oxybutynin chloride
Labeler / Manufacturer: TruPharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190101

FDA application: ANDA210125

## 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:"52817-260"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52817-260
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7c497c6c-2448-2c80-e053-2991aa0ab8c7