# Oxybutynin Chloride

NDC: 68788-8141
Generic name: Oxybutynin Chloride
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220211

FDA application: ANDA209335

## Active ingredients

- OXYBUTYNIN CHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8141"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8141
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0e002fe8-fa3f-4a7d-84df-0c6e031e6ae4