NDC 0832-6032
Fluoxetine hydrochloride 20 mg per 5 mL for solution
On the label: Upsher-Smith Laboratories, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| AptaPharma Inc. | Pennsauken, NJ, United States | Makes it | Problems found, fixed voluntarilyAug 14, 2026 · 5 inspections |
Product details
- Generic drug
- Fluoxetine: every company that makes it
- Form
- for solution, oral
- Strength
- 20 mg per 5 mL
- Approval
- ANDA ANDA216953
- On the market since
- Nov 15, 2022
- Package NDCs
0832-6032-12- Official label
- DailyMed (National Library of Medicine), updated Oct 6, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?