Class II · Moderate risk
Eletriptan Hydrobromide Tablets 20 mg* 6
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 59651-0104-69 recalled?
Eletriptan Hydrobromide · 1 BLISTER PACK in 1 CARTON (59651-104-69) / 6 TABLET, FILM COATED in 1 BLISTER PACK (59651-104-06)
Yes — this exact package was recalled
1 FDA recall names the code 59651-0104-69 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
- Eletriptan Hydrobromide
- Strength
- ELETRIPTAN HYDROBROMIDE 20 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Aurobindo Pharma Limited
- Type
- Human Prescription Drug
- Product code
- 59651-0104
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
- 59651-0137 Nebivolol 1
- 59651-0145 See recall 1
- 59651-0616 Rufinamide 1
- 59651-0617 Rufinamide 1
Free recall alerts
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