Class III · Low risk
Trokendi XR
Failed dissolution specifications.
National Drug Code
Is NDC 17772-0102-30 recalled?
Trokendi XR · 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (17772-102-30)
Yes — this exact package was recalled
1 FDA recall names the code 17772-0102-30 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.
1 of these recalls is still ongoing.
- Active ingredient
- topiramate
- Strength
- TOPIRAMATE 50 mg/1
- Form
- Capsule, Extended Release · Oral
- Labeler
- Supernus Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 17772-0102
Recalls naming this package
Class II · Moderate risk
Trokendi XR
Superpotent Drug: Failure of assay specifications in the capsule.
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
- 17772-0101 Trokendi XR 1
- 17772-0103 Trokendi XR 1
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