# oxycodone and acetaminophen

NDC: 72887-683
Generic name: oxycodone and acetaminophen tablets
Labeler / Manufacturer: FH2 Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200701

FDA application: ANDA040608

## Active ingredients

- ACETAMINOPHEN: 300 mg/1
- OXYCODONE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72887-683"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72887-683
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=88d97caf-bcf5-3cde-e053-2995a90acf4a