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

Is NDC 0093-7442-56 recalled?

Fluvastatin · 30 CAPSULE in 1 BOTTLE (0093-7442-56)

Yes — this exact package was recalled

1 FDA recall names the code 0093-7442-56 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
Fluvastatin
Strength
FLUVASTATIN SODIUM 20 mg/1
Form
Capsule · Oral
Labeler
Teva Pharmaceuticals USA, Inc.
Type
Human Prescription Drug
Product code
0093-7442

Recalls naming this package

Class II ยท Moderate risk

Fluvastatin Capsules USP

Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, Inc. is voluntarily recalling one lot of Fluvastatin Capsules USP, 20 mg due to a customer complaint trend regarding capsule breakage.

Terminated Failed specification Teva Pharmaceuticals USA NDC 0093-7442-56 D-1430-2014

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