# Oxybutynin Chloride

NDC: 66267-642
Generic name: Oxybutynin Chloride
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20171115

FDA application: ANDA209823

## Active ingredients

- OXYBUTYNIN CHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"66267-642"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=66267-642
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8e830697-a6d3-13ed-e053-2995a90acb11