NDC 60687-406
Oxycodone Hydrochloride 5 mg per 5 mL solution
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-0390.
Where the pills inside were 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.
Repackaging site
- American Health Packaging, Columbus, OH, United States · tests it and repackages it
Recalls
- Feb 22, 2022 · Class II · American Health Packaging
Impurity failure at 0-time of the repackaged lot.
Lots: Lot# 1004276, Exp 11/30/2022 - 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
- Apr 22, 2019
- Package NDCs
60687-406-4060687-406-4660687-406-6760687-406-77- Official label
- DailyMed (National Library of Medicine), updated Mar 20, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?