# Oxycodone and Acetaminophen

NDC: 42858-102
Generic name: Oxycodone and Acetaminophen
Labeler / Manufacturer: Rhodes Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140828

FDA application: ANDA201278

## Active ingredients

- ACETAMINOPHEN: 325 mg/1
- OXYCODONE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42858-102"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42858-102
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5999f3c3-3225-4d24-82cd-0b8d7a309587