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

Is NDC 57664-0502-89 recalled?

Tizanidine · 150 TABLET in 1 BOTTLE (57664-502-89)

Yes — this exact package was recalled

1 FDA recall names the code 57664-0502-89 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
Tizanidine
Strength
TIZANIDINE HYDROCHLORIDE 2 mg/1
Form
Tablet · Oral
Labeler
Sun Pharmaceutical Industries, Inc.
Type
Human Prescription Drug
Product code
57664-0502

Recalls naming this package

Class II ยท Moderate risk

tiZANidine HCL Tablet

Labeling:Label Mixup; tiZANidine HCL Tablet, 2 mg may be potentially mislabeled as NICOTINE POLACRILEX, Lozenge, 2 mg, NDC 37205098769, Pedigree: AD70700_4, EXP: 5/29/2014; NIFEdipine ER, Tablet, 60 mg, NDC 00591319401, Pedigree: W003729, EXP: 6/26/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-627-2014

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