Class II ยท Moderate risk
Briviact (brivaracetam)
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 50474-0570-66 recalled?
Briviact · 1 BOTTLE in 1 CARTON (50474-570-66) / 60 TABLET, FILM COATED in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 50474-0570-66 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
- brivaracetam
- Strength
- BRIVARACETAM 50 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- UCB, Inc.
- Type
- Human Prescription Drug · DEA CV
- Product code
- 50474-0570
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
- 50474-0710 Cimzia 2
- 50474-0597 Keppra 1
Free recall alerts
Know the day your medication is recalled
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