NDC 68071-3400
Diethylpropion Hydrochloride 25 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-044.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Kvk-Tech, Inc. | Newtown, PA, United States | Makes it | Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Diethylpropion: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA201212
- On the market since
- Dec 27, 2010
- Package NDCs
68071-3400-068071-3400-168071-3400-268071-3400-368071-3400-468071-3400-568071-3400-7- Official label
- DailyMed (National Library of Medicine), updated Feb 4, 2025
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