NDC 70954-600

Fluoxetine Hydrochloride 20 mg per 5 mL solution

On the label: ANI Pharmaceuticals, Inc..

Where it's 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 ANI Pharmaceuticals, Inc. names for other drugs.

Product details

Generic drug
Fluoxetine: every company that makes it
Form
solution, oral
Strength
20 mg per 5 mL
Approval
ANDA ANDA216448
On the market since
Nov 9, 2022
Package NDCs
70954-600-10
Official label
DailyMed (National Library of Medicine), updated Jan 5, 2026

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