Class III · Low risk
Xiidra (lifitegrast ophthalmic solution)
Failed Impurities/Degradation Specifications.
National Drug Code
Is NDC 0078-0911-05 recalled?
Xiidra
Yes — this exact package was recalled
1 FDA recall names the code 0078-0911-05 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
- Lifitegrast
- Strength
- LIFITEGRAST 50 mg/mL
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Novartis Pharmaceuticals Corporation
- Type
- Human Prescription Drug
- Product code
- 0078-0911
Recalls naming this package
Class III · Low risk
Xiidra (lifitegrast ophthalmic solution)
Failed Impurities/Degradation Specifications.
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
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