# OXYCODONE HYDROCHLORIDE

NDC: 0121-0827
Generic name: OXYCODONE HYDROCHLORIDE
Labeler / Manufacturer: PAI Holdings, LLC dba PAI Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20190408

FDA application: ANDA206914

## Active ingredients

- OXYCODONE HYDROCHLORIDE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0121-0827"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-0827
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=73b063b5-24b7-40bf-bc2a-c0e1bfaf61d1