NDC 68071-3484

Fluoxetine 20 mg capsule

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-029.

United States: 1India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.East Brunswick, NJ, United StatesMakes it, tests it and packages it No problems foundSep 19, 2023 · 10 inspections
Sidmak Laboratories (India) Private LimitedDehradun, IndiaMakes it No problems foundMay 13, 2023 · 5 inspections

Repackaging site

Product details

Generic drug
Fluoxetine: every company that makes it
Form
capsule
Strength
20 mg
Approval
ANDA ANDA201336
On the market since
Aug 8, 2021
Package NDCs
68071-3484-3 68071-3484-6
Official label
DailyMed (National Library of Medicine), updated Oct 13, 2023

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