# Oxybutynin Chloride Extended Release

NDC: 43353-322
Generic name: Oxybutynin Chloride
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160309

FDA application: ANDA078503

## 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:"43353-322"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43353-322
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=02ff3be7-fc5c-4b91-8c67-ecdf6e19c42a