NDC 65862-062

Metoprolol Tartrate 25 mg tablet, film coated

On the label: Aurobindo Pharma Limited.

India: 1United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMedchal, IndiaMakes it and tests it Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action
Aurolife Pharma LLCDayton, NJ, United StatesMakes it and tests it Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 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
Metoprolol: every company that makes it
Form
tablet, film coated, oral
Strength
25 mg
Approval
ANDA ANDA077739
On the market since
Sep 11, 2007
Package NDCs
65862-062-01 65862-062-99
Official label
DailyMed (National Library of Medicine), updated Feb 13, 2024

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