# Oxycodone Hydrochloride

NDC: 10702-023
Generic name: Oxycodone Hydrochloride
Labeler / Manufacturer: KVK-TECH, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20150820

FDA application: ANDA202773

## 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:"10702-023"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10702-023
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=338b5391-e5f7-40a2-8b15-57f47cbc4813