# oxycodone hydrochloride

NDC: 0054-0390
Generic name: oxycodone hydrochloride
Labeler / Manufacturer: Hikma Pharmceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20140904

FDA application: ANDA204037

## 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:"0054-0390"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-0390
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d8e87c66-f872-4e1d-9ade-ef11490af63b