# Oxycodone Hydchloride

NDC: 49999-899
Generic name: Oxycodone Hydchloride
Labeler / Manufacturer: Quality Care Products LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20111220
Marketing ended: 20270630
FDA application: ANDA091393

## 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:"49999-899"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49999-899
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b9847cc7-67a2-408d-93cf-f9cf420346dd