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

Is NDC 0591-0404-01 recalled?

Verapamil Hydrochloride · 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0404-01)

Yes — this exact package was recalled

1 FDA recall names the code 0591-0404-01 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
Verapamil Hydrochloride
Strength
VERAPAMIL HYDROCHLORIDE 40 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Actavis Pharma, Inc.
Type
Human Prescription Drug
Product code
0591-0404

Recalls naming this package

Class II · Moderate risk

Verapamil HCL

Labeling: Label Mixup: VERAPAMIL HCL, Tablet, 40 mg may have potentially been mislabeled as one of the following drugs: ATORVASTATIN CALCIUM, Tablet, 10 mg, NDC 00378201577, Pedigree: W003095, EXP: 6/12/2014; TACROLIMUS, Capsule, 1 mg, NDC 00781210301, Pedigree: W003352, EXP: 3/31/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-962-2014

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