NDC 51655-608
Topiramate 100 mg tablet, film coated
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-109.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Goa, India | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Apr 5, 2013 · Class III · Glenmark Generics Inc., USA
Chemical Contamination: Topiramate Tablets is being recalled due to complaints related to an off - odor. described as moldy, musty or fishy in nature.
Lots: Lot# 02123782, Exp 11/14
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
- tablet, film coated, oral
- Strength
- 100 mg
- Approval
- ANDA ANDA077627
- On the market since
- Feb 2, 2015
- Package NDCs
51655-608-2651655-608-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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