# Oxycodone Hydrochloride

NDC: 65162-047
Generic name: Oxycodone
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20121030

FDA application: ANDA203638

## Active ingredients

- OXYCODONE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65162-047"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-047
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=094b64b3-cd32-4de5-afb6-ea00d9caad74