# Oxycodone Hydrochloride

NDC: 63629-2104
Generic name: Oxycodone Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20151013

FDA application: ANDA204979

## Active ingredients

- OXYCODONE HYDROCHLORIDE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-2104"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-2104
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e0079cc8-3642-47f0-9d14-28fd8f212c21