# OXYCODONE AND ACETAMINOPHEN

NDC: 71335-9675
Generic name: oxycodone and acetaminophen
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190601

FDA application: ANDA207510

## Active ingredients

- ACETAMINOPHEN: 325 mg/1
- OXYCODONE HYDROCHLORIDE: 7.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-9675"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-9675
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3339d3bd-b416-4c5b-8984-0c376544d8a9