NDC 72789-208
Phentermine Hydrochloride 37.5 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from TAGI Pharma, Inc.'s NDC 51224-101.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Elite Laboratories, Inc. | Northvale, NJ, United States | Makes it and labels it | Problems found, fixed voluntarilyAug 1, 2025 · 12 inspections, 1 with FDA action |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Phentermine: every company that makes it
- Form
- tablet
- Strength
- 37.5 mg
- Approval
- ANDA ANDA200272
- On the market since
- Mar 8, 2011
- Package NDCs
72789-208-01- Official label
- DailyMed (National Library of Medicine), updated Jan 18, 2024
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