NDC 0054-0390
oxycodone hydrochloride 5 mg per 5 mL solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Hikma Pharmaceuticals USA Inc. names for other drugs.
Recalls
- May 19, 2016 · Class III · West-Ward Columbus Inc
Failed Impurities/Degradation Specification; 9 month stability
Lots: Lot #560185A; Exp. 6/30/2017
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Oxycodone: every company that makes it
- Form
- solution, oral
- Strength
- 5 mg per 5 mL
- Approval
- ANDA ANDA204037
- On the market since
- Sep 4, 2014
- Package NDCs
0054-0390-410054-0390-63- Official label
- DailyMed (National Library of Medicine), updated Jan 20, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?