NDC 53002-1796
Fluoxetine Hydrochloride 10 mg tablet
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-998.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Nagpur, India | Makes it and packages it | Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections |
Repackaging site
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Product details
- Generic drug
- Fluoxetine: every company that makes it
- Form
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA211653
- On the market since
- Aug 7, 2019
- Package NDCs
53002-1796-053002-1796-3- Official label
- DailyMed (National Library of Medicine), updated Jan 31, 2023
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