# Oxycodone and Acetaminophen

NDC: 71205-329
Generic name: Oxycodone and Acetaminophen
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170411

FDA application: ANDA207419

## 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:"71205-329"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-329
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=484a4323-0758-439d-844f-f04d7e5ef6f3