# Oxycodone and Acetaminophen

NDC: 49999-852
Generic name: Oxycodone and Acetaminophen
Labeler / Manufacturer: Quality Care products LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100610
Marketing ended: 20290228
FDA application: ANDA087463

## 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:"49999-852"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49999-852
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3f2b939c-2206-469b-85a4-b0ee9ba25be8