NDC 69097-299

duloxetine 60 mg capsule, delayed release

On the label: Cipla USA., Inc..

India: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Inventia Healthcare LimitedThane, IndiaMakes it Problems found, fixed voluntarilyFeb 12, 2025 · 4 inspections
Zydus Lifesciences LimitedAnkleshwar, IndiaMakes the active ingredient, tests it, packages it and labels it No problems foundMar 14, 2025 · 4 inspections

Product details

Generic drug
Duloxetine: every company that makes it
Form
capsule, delayed release
Strength
60 mg
Approval
ANDA ANDA202336
On the market since
Dec 5, 2015
Package NDCs
69097-299-02 69097-299-03 69097-299-05 69097-299-15
Official label
DailyMed (National Library of Medicine), updated Apr 26, 2016

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