NDC 68462-199

Telmisartan 20 mg tablet

On the label: Glenmark Pharmaceuticals Inc., USA.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Glenmark Pharmaceuticals LimitedGoa, IndiaMakes it and tests it Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action

Product details

Generic drug
Telmisartan: every company that makes it
Form
tablet, oral
Strength
20 mg
Approval
ANDA ANDA090032
On the market since
Jul 7, 2014
Package NDCs
68462-199-01 68462-199-13 68462-199-30 68462-199-90 68462-199-96
Official label
DailyMed (National Library of Medicine), updated Jan 28, 2026

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