NDC 59651-279

Duloxetine 20 mg capsule, delayed release

On the label: Aurobindo Pharma Limited.

India: 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

Product details

Generic drug
Duloxetine: every company that makes it
Form
capsule, delayed release, oral
Strength
20 mg
Approval
ANDA ANDA090778
On the market since
Dec 11, 2013
Package NDCs
59651-279-10 59651-279-60 59651-279-71 59651-279-78 59651-279-99
Official label
DailyMed (National Library of Medicine), updated Nov 7, 2024

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