# OXYCODONE HYDROCHLORIDE

NDC: 70752-137
Generic name: OXYCODONE HYDROCHLORIDE
Labeler / Manufacturer: QUAGEN PHARMACEUTICALS LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20210602

FDA application: ANDA213761

## Active ingredients

- OXYCODONE HYDROCHLORIDE: 100 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70752-137"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70752-137
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=391701e5-2035-43fa-91ce-d27a1af19492