NDC 72189-133

Armodafinil 250 mg tablet

On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Aurobindo Pharma Limited's NDC 65862-807.

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
Armodafinil: every company that makes it
Form
tablet, oral
Strength
250 mg
Approval
ANDA ANDA206069
On the market since
Oct 15, 2020
Package NDCs
72189-133-30
Official label
DailyMed (National Library of Medicine), updated Jan 20, 2025

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