NDC 72789-260
AMLODIPINE BESYLATE2.5 mg 2.5 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-021.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Oxford Pharmaceuticals, LLC | Birmingham, AL, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Amlodipine: every company that makes it
- Form
- tablet, oral
- Strength
- 2.5 mg
- Approval
- ANDA ANDA078414
- On the market since
- Oct 1, 2021
- Package NDCs
72789-260-3072789-260-6072789-260-9072789-260-95- Official label
- DailyMed (National Library of Medicine), updated Jul 17, 2026
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