NDC 71335-0845

Olmesartan Medoxomil and Hydrochlorothiazide 40 mg / 12.5 mg tablet, film coated

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Aurobindo Pharma Limited's NDC 65862-780.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Hydrochlorothiazide and Olmesartan: every company that makes it
Form
tablet, film coated, oral
Strength
40 mg / 12.5 mg
Approval
ANDA ANDA205391
On the market since
Apr 24, 2017
Package NDCs
71335-0845-1 71335-0845-2 71335-0845-3
Official label
DailyMed (National Library of Medicine), updated Jul 14, 2025

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