NDC 65862-193

Fluoxetine 20 mg capsule

On the label: Aurobindo Pharma Limited.

India: 3

Where it's made

FactoryWhereRoleLast FDA inspection
Apl Healthcare LimitedTirupati, IndiaMakes it and tests it Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections
Aurobindo Pharma LimitedMedchal, IndiaMakes it and tests it Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Product details

Generic drug
Fluoxetine: every company that makes it
Form
capsule, oral
Strength
20 mg
Approval
ANDA ANDA078619
On the market since
Jan 31, 2008
Package NDCs
65862-193-01 65862-193-05 65862-193-30 65862-193-99
Official label
DailyMed (National Library of Medicine), updated Oct 29, 2026

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