# Oxycodone and Acetaminophen

NDC: 65162-207
Generic name: Oxycodone and Acetaminophen
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20131101

FDA application: ANDA040778

## Active ingredients

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

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65162-207"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-207
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c5cc2e88-aa00-46bd-91dc-901c3a7c899c