# OXYCODONE AND ACETAMINOPHEN

NDC: 10702-238
Generic name: oxycodone and acetaminophen
Labeler / Manufacturer: KVK-Tech, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20191205

FDA application: ANDA211499

## Active ingredients

- ACETAMINOPHEN: 325 mg/5mL
- OXYCODONE HYDROCHLORIDE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10702-238"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10702-238
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9986aa04-c976-4654-8ad7-b97d2eecea93