# Oxybutynin Chloride Extended Release

NDC: 82804-095
Generic name: Oxybutynin Chloride
Labeler / Manufacturer: Proficient Rx LP
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: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82804-095"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82804-095
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7d2332b4-9e48-4bb2-a2c3-75e16e1d455b