# oxybutynin

NDC: 68382-256
Generic name: oxybutynin
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20170810

FDA application: ANDA202332

## Active ingredients

- OXYBUTYNIN CHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68382-256"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-256
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c042bf06-79a3-4dc7-ae05-3ef3cfae9d44