Class II ยท Moderate risk
C-*Albumin Eye Drop 10% S
Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.
National Drug Code
Is NDC 44206-0251-05 recalled?
AlbuRx · 1 VIAL, GLASS in 1 CARTON (44206-251-05) / 50 mL in 1 VIAL, GLASS (44206-251-90)
Yes — this exact package was recalled
1 FDA recall names the code 44206-0251-05 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
- Albumin (human)
- Strength
- ALBUMIN HUMAN 12.5 g/50mL
- Form
- Solution · Intravenous
- Labeler
- CSL Behring AG
- Type
- Plasma Derivative
- Product code
- 44206-0251
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.
Free recall alerts
Know the day your medication is recalled
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