NDC 17224-672
benzphetamine hydrochloride 50 mg tablet
On the label: Calvin Scott & Co., Inc.. It's repackaged: Calvin Scott & Co., Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-040.
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 |
Product details
- Generic drug
- Benzphetamine: every company that makes it
- Form
- tablet, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA090968
- On the market since
- Jan 1, 2010
- Package NDCs
17224-672-3017224-672-60- Official label
- DailyMed (National Library of Medicine), updated Mar 2, 2023
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