Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 23155-0050-01 recalled?

Felodipine · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23155-050-01)

Yes — this exact package was recalled

1 FDA recall names the code 23155-0050-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Felodipine
Strength
FELODIPINE 10 mg/1
Form
Tablet, Extended Release · Oral
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Type
Human Prescription Drug
Product code
23155-0050

Recalls naming this package

Class III ยท Low risk

Felodipine Extended Release Tablets

Failed impurities/ degradation specifications: Out of specification impurity results were observed during routine testing of stability samples for the impurity Felodipine Related compound A

Terminated Impurity / degradation Heritage Pharmaceuticals Inc NDC 23155-050-01 D-0108-2021

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler