NDC 33342-173

OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE 20 mg / 12.5 mg tablet, film coated

On the label: Macleods Pharmaceuticals Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Macleods Pharmaceuticals LimitedDaman, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyMay 26, 2023 · 4 inspections

Product details

Generic drug
Hydrochlorothiazide and Olmesartan: every company that makes it
Form
tablet, film coated, oral
Strength
20 mg / 12.5 mg
Approval
ANDA ANDA204801
On the market since
Jun 2, 2023
Package NDCs
33342-173-07 33342-173-10 33342-173-12 33342-173-44
Official label
DailyMed (National Library of Medicine), updated May 22, 2025

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