# Oxybutynin Chloride

NDC: 10702-201
Generic name: Oxybutynin Chloride
Labeler / Manufacturer: KVK-Tech, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20171222

FDA application: ANDA209335

## 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:"10702-201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10702-201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f99fdfe8-a980-4a72-bc99-aa2ce0bdfd86