# OXYCODONE AND ACETAMINOPHEN

NDC: 0406-0522
Generic name: oxycodone hydrochloride and acetaminophen
Labeler / Manufacturer: SpecGx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20040630

FDA application: ANDA040545

## 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:"0406-0522"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0406-0522
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2137f1a-b49a-40bd-97ac-cd6b36e295f4