NDC 17772-102
Trokendi XR 50 mg capsule, extended release
On the label: Supernus Pharmaceuticals, Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Supernus Pharmaceuticals, Inc. names for other drugs.
Recalls
- Aug 31, 2026 · Class III · Supernus Pharmaceuticals, Inc.
Failed dissolution specifications.
Lots: Lot# 2145283, Exp Date: 31-Mar-2030. - Jul 12, 2016 · Class II · Supernus Pharmaceuticals, Inc.
Superpotent Drug: Failure of assay specifications in the capsule.
Lots: Lot # 426636, Exp 4/22/18
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Topiramate: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 50 mg
- Approval
- NDA NDA201635
- On the market since
- Aug 16, 2013
- Package NDCs
17772-102-0117772-102-0717772-102-1017772-102-1217772-102-1517772-102-3017772-102-70- Official label
- DailyMed (National Library of Medicine), updated Oct 5, 2026
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