# Oxycodone Hydrochloride

NDC: 72865-128
Generic name: Oxycodone Hydrochloride
Labeler / Manufacturer: XLCare Pharmaceuticals, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200225

FDA application: ANDA207418

## Active ingredients

- OXYCODONE HYDROCHLORIDE: 15 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72865-128"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72865-128
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e5c8e72d-4ac5-4ca3-9557-6a659d4d8338