Class I · High risk
Ibuprofen Lysine Injection
Presence of Particulate Matter
National Drug Code
Is NDC 39822-1030-01 recalled?
Ibuprofen Lysine
Yes — this exact package was recalled
1 FDA recall names the code 39822-1030-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Ibuprofen Lysine
- Strength
- IBUPROFEN LYSINE 10 mg/mL
- Form
- Solution · Intravenous
- Labeler
- XGen Pharmaceuticals DJB, Inc.
- Type
- Human Prescription Drug
- Product code
- 39822-1030
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 39822-2000 Clonidine 2
- 39822-0250 Cyclophosphamide 1
- 39822-0255 Cyclophosphamide 1
- 39822-0310 See recall 1
- 39822-4000 Levetiracetam 1
Free recall alerts
Know the day your medication is recalled
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