# Oxybutynin Chloride

NDC: 17856-0149
Generic name: Oxybutynin Chloride
Labeler / Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SYRUP
Routes: ORAL
Marketing started: 19960329

FDA application: ANDA074520

## Active ingredients

- OXYBUTYNIN CHLORIDE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17856-0149"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0149
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fe4ed76b-0009-455f-be30-47e80fc1afdf