# OXYCODONE HYDROCHLORIDE

NDC: 67296-0425
Generic name: oxycodone hydrochloride
Labeler / Manufacturer: RedPharm Drug, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20090730

FDA application: ANDA076758

## Active ingredients

- OXYCODONE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67296-0425"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67296-0425
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=92614a3a-331d-16ad-e053-2a95a90a47cc