NDC 67877-263

Duloxetine 20 mg capsule, delayed release

On the label: Ascend Laboratories, LLC.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Alkem Laboratories LimitedAmaliya Daman, IndiaMakes it, tests it and packages it No problems foundAug 30, 2019 · 6 inspections

Product details

Generic drug
Duloxetine: every company that makes it
Form
capsule, delayed release, oral
Strength
20 mg
Approval
ANDA ANDA203197
On the market since
May 1, 2012
Package NDCs
67877-263-01 67877-263-10 67877-263-30 67877-263-60 67877-263-90
Official label
DailyMed (National Library of Medicine), updated Aug 11, 2025

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