NDC 23155-050
Felodipine 10 mg tablet, extended release
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| USV Private Limited | Daman, India | Makes it | Serious problems, FDA actionApr 17, 2026 · 8 inspections, 3 with FDA action |
Recalls
- Oct 23, 2020 · Class III · Heritage Pharmaceuticals Inc
Failed impurities/ degradation specifications: Out of specification impurity results were observed during routine testing of stability samples for the impurity Felodipine Related compound A
Lots: Lot #: 18029979, Exp 1/2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Felodipine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA201964
- On the market since
- Nov 8, 2013
- Package NDCs
23155-050-01- Official label
- DailyMed (National Library of Medicine), updated Aug 11, 2026
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