NDC 70518-3752

Fluoxetine 10 mg capsule

On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 50111-647.

Where the pills inside were made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Fluoxetine: every company that makes it
Form
capsule, oral
Strength
10 mg
Approval
ANDA ANDA076001
On the market since
Jun 8, 2023
Package NDCs
70518-3752-0
Official label
DailyMed (National Library of Medicine), updated Apr 15, 2026

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