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

Is NDC 0006-0112-31 recalled?

Januvia · 30 TABLET, FILM COATED in 1 BOTTLE (0006-0112-31)

Yes — this exact package was recalled

1 FDA recall names the code 0006-0112-31 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
sitagliptin
Strength
SITAGLIPTIN PHOSPHATE 50 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Merck Sharp & Dohme LLC
Type
Human Prescription Drug
Product code
0006-0112

Recalls naming this package

Class II ยท Moderate risk

sitaGLIPtin PHOSPHATE

Labeling: Label Mixup: sitaGLIPtin PHOSPHATE, Tablet, 50 mg may be potentially mis-labeled as one of the following drugs: LACTOBACILLUS, Tablet, 0 mg, NDC 64980012950, Pedigree: AD62992_1, EXP: 5/23/2014; CYANOCOBALAMIN, Tablet, 500 mcg, NDC 00536355101, Pedigree: W002860, EXP: 6/7/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-774-2014

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