NDC 70756-812

Olmesartan Medoxomil and Hydrochlorothiazide 20 mg / 12.5 mg tablet

On the label: Lifestar Pharma LLC..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Umedica Laboratories Private LimitedVapi, IndiaMakes it, tests it and packages it Problems found, fixed voluntarilyMar 29, 2024 · 4 inspections

Product details

Generic drug
Hydrochlorothiazide and Olmesartan: every company that makes it
Form
tablet, oral
Strength
20 mg / 12.5 mg
Approval
ANDA ANDA208847
On the market since
Oct 1, 2020
Package NDCs
70756-812-12 70756-812-30 70756-812-51 70756-812-90
Official label
DailyMed (National Library of Medicine), updated Oct 23, 2026

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