NDC 65862-602

Modafinil 200 mg tablet

On the label: Aurobindo Pharma Limited.

India: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Apl Healthcare LimitedMahabubnagar, IndiaMakes it and tests it No problems foundJan 18, 2023 · 2 inspections
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Product details

Generic drug
Modafinil: every company that makes it
Form
tablet, oral
Strength
200 mg
Approval
ANDA ANDA202566
On the market since
Sep 27, 2012
Package NDCs
65862-602-01 65862-602-05 65862-602-30 65862-602-90
Official label
DailyMed (National Library of Medicine), updated May 27, 2024

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