# oxybutynin

NDC: 70771-1088
Generic name: oxybutynin
Labeler / Manufacturer: Zydus Lifesciences Limited
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: 15 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1088"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1088
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f405a774-bd91-4513-b7c7-c44f0596d988