NDC 70518-4780

OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE 25 mg / 40 mg tablet, film coated

On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Macleods Pharmaceuticals Limited's NDC 33342-175.

India: 1

Where the pills inside were 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
25 mg / 40 mg
Approval
ANDA ANDA204801
On the market since
Oct 25, 2026
Package NDCs
70518-4780-0
Official label
DailyMed (National Library of Medicine), updated Oct 26, 2026

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