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

Is NDC 62175-0107-01 recalled?

isosorbide mononitrate · 100 TABLET in 1 BOTTLE (62175-107-01)

Yes — this exact package was recalled

1 FDA recall names the code 62175-0107-01 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
isosorbide mononitrate
Strength
ISOSORBIDE MONONITRATE 20 mg/1
Form
Tablet · Oral
Labeler
Lannett Company, Inc.
Type
Human Prescription Drug
Product code
62175-0107

Recalls naming this package

Class II · Moderate risk

Isosorbide Mononitrate

Labeling:Label Mixup; ISOSORBIDE MONONITRATE Tablet, 20 mg may be potentially mislabeled as COLCHICINE, Tablet, 0.6 mg, NDC 64764011907, Pedigree: AD52778_22, EXP: 5/20/2014; LOSARTAN POTASSIUM, Tablet, 25 mg, NDC 16714058102, Pedigree: AD67989_7, EXP: 5/28/2014; SODIUM CHLORIDE, Tablet, 1 mg, NDC 00223176001, Pedigree: W002611, EXP: 6/4/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-670-2014

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