NDC 65841-799

Duloxetine 20 mg capsule, delayed release

On the label: Cadila Healthcare Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action

Product details

Generic drug
Duloxetine: every company that makes it
Form
capsule, delayed release, oral
Strength
20 mg
Approval
ANDA ANDA090739
On the market since
May 27, 2014
Package NDCs
65841-799-06 65841-799-14 65841-799-16
Official label
DailyMed (National Library of Medicine), updated Nov 28, 2024

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