# oxycodone hydrochloride and acetaminophen

NDC: 72887-648
Generic name: oxycodone hydrochloride and acetaminophen
Labeler / Manufacturer: FH2 Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20200301

FDA application: ANDA202142

## Active ingredients

- ACETAMINOPHEN: 300 mg/5mL
- OXYCODONE HYDROCHLORIDE: 10 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72887-648"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72887-648
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=96b0067e-aabe-df4f-e053-2995a90a4a86