# Oxycodone Hydrochloride

NDC: 63629-1929
Generic name: Oxycodone Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170808

FDA application: ANDA207418

## Active ingredients

- OXYCODONE HYDROCHLORIDE: 30 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-1929"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-1929
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b6d0f446-cc77-443a-bcee-d5504ab3e5c9