NDC 70954-860

duloxetine 20 mg capsule, delayed release

On the label: ANI Pharmaceuticals, Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Inventia Healthcare LimitedThane, IndiaMakes it Problems found, fixed voluntarilyFeb 12, 2025 · 4 inspections

Product details

Generic drug
Duloxetine: every company that makes it
Form
capsule, delayed release, oral
Strength
20 mg
Approval
ANDA ANDA202336
On the market since
Dec 5, 2015
Package NDCs
70954-860-30
Official label
DailyMed (National Library of Medicine), updated Oct 15, 2026

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