Class II · Moderate risk
Gabapentin Capsules
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
National Drug Code
Is NDC 55154-3363-00 recalled?
Gabapentin · 10 BLISTER PACK in 1 BAG (55154-3363-0) / 1 CAPSULE in 1 BLISTER PACK
Yes — this exact package was recalled
2 FDA recalls name the code 55154-3363-00 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.
2 of these recalls are still ongoing.
- Active ingredient
- Gabapentin
- Strength
- GABAPENTIN 100 mg/1
- Form
- Capsule · Oral
- Labeler
- Cardinal Health 107, LLC
- Type
- Human Prescription Drug
- Product code
- 55154-3363
Recalls naming this package
Class II · Moderate risk
Gabapentin Capsules
Defective container; blister packaging inadequately sealed.
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
- 55154-3543 Enoxaparin Sodium 1
- 55154-3558 Levothyroxine Sodium 1
- 55154-3559 Levothyroxine Sodium 1
- 55154-3560 Levothyroxine Sodium 1
- 55154-3562 Levothyroxine Sodium 1
- 55154-3563 Levothyroxine Sodium 1
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