NDC 68382-138

topiramate 25 mg tablet, film coated

On the label: Zydus Pharmaceuticals (USA) Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action

Recalls

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
25 mg
Approval
ANDA ANDA078235
On the market since
Mar 27, 2009
Package NDCs
68382-138-01 68382-138-05 68382-138-14 68382-138-16
Official label
DailyMed (National Library of Medicine), updated Apr 15, 2026

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