Oxford Pharmaceuticals, LLC
Birmingham, AL, United States · makes it, tests it and packages it
Problems found, fixed voluntarily Last FDA inspection Nov 3, 2023. 3 inspections on record.
NDC 72789-262
AMLODIPINE BESYLATE10 mg 10 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc..
It's a repackaged product: PD-Rx Pharmaceuticals, Inc. rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-023.
Where the pills inside were made
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Amlodipine: see every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA078414
- On the market since
- Oct 1, 2021
- Package NDCs
72789-262-3072789-262-6072789-262-9072789-262-95- Official label
- DailyMed (National Library of Medicine), updated Jul 17, 2026
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