NDC 17856-0390
oxycodone hydrochloride 5 mg per 5 mL solution
On the label: Atlantic Biologicals Corps.. It's repackaged: Atlantic Biologicals Corps. 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
- Atlantic Biologicals Corps, Location not on file · repackages it
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
- Strength
- 5 mg per 5 mL
- Approval
- ANDA ANDA204037
- On the market since
- Sep 4, 2014
- Package NDCs
17856-0390-117856-0390-217856-0390-3- Official label
- DailyMed (National Library of Medicine), updated May 15, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?