Class II ยท Moderate risk
Rufinamide Tablets
cGMP deviations: Batch was released prior to approval.
National Drug Code
Is NDC 59651-0617-08 recalled?
Rufinamide · 120 TABLET, FILM COATED in 1 BOTTLE (59651-617-08)
Yes — this exact package was recalled
1 FDA recall names the code 59651-0617-08 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
- rufinamide
- Strength
- RUFINAMIDE 400 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Aurobindo Pharma Limited
- Type
- Human Prescription Drug
- Product code
- 59651-0617
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
- 59651-0144 See recall 2
- 59651-0032 Ibuprofen 1
- 59651-0104 Eletriptan Hydrobromide 1
- 59651-0137 Nebivolol 1
- 59651-0145 See recall 1
- 59651-0616 Rufinamide 1
Free recall alerts
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