NDC 33342-192

AMLODIPINE and OLMESARTAN medoxomil 10 mg / 20 mg tablet, film coated

On the label: Macleods Pharmaceuticals Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Macleods Pharmaceuticals LimitedDistrict Solan, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 with FDA action

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Amlodipine and Olmesartan: every company that makes it
Form
tablet, film coated, oral
Strength
10 mg / 20 mg
Approval
ANDA ANDA206884
On the market since
Oct 27, 2016
Package NDCs
33342-192-07 33342-192-10 33342-192-12 33342-192-44
Official label
DailyMed (National Library of Medicine), updated Jan 3, 2026

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