NDC 68071-3453
AMLODIPINE BESYLATE10 mg 10 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-023.
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
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Amlodipine: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA078414
- On the market since
- Oct 1, 2021
- Package NDCs
68071-3453-268071-3453-368071-3453-9- Official label
- DailyMed (National Library of Medicine), updated Mar 26, 2024
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