Class II · Moderate risk
Levetiracetam Tablets
Adulterated Presence of Foreign Tablets: Pharmaceutical manufacturer may have distributed foreign tablets in bottles of Levetiracetam Tablets, USP 500 mg.
National Drug Code
Is NDC 0378-5615-05 recalled?
Levetiracetam · 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5615-05)
Yes — this exact package was recalled
1 FDA recall names the code 0378-5615-05 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
- levetiracetam
- Strength
- LEVETIRACETAM 500 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Mylan Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 0378-5615
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
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