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 69584-021
AMLODIPINE BESYLATE2.5 mg 2.5 mg tablet
On the label: Oxford Pharmaceuticals, LLC.
Where it's made
Product details
- Generic drug
- Amlodipine: see every company that makes it
- Form
- tablet, oral
- Strength
- 2.5 mg
- Approval
- ANDA ANDA078414
- On the market since
- Oct 1, 2021
- Package NDCs
69584-021-0969584-021-5069584-021-90- Official label
- DailyMed (National Library of Medicine), updated Mar 28, 2026
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