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

Is NDC 0006-0227-61 recalled?

Isentress · 60 TABLET, FILM COATED in 1 BOTTLE (0006-0227-61)

Yes — this exact package was recalled

1 FDA recall names the code 0006-0227-61 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
Raltegravir
Strength
RALTEGRAVIR POTASSIUM 400 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Merck Sharp & Dohme LLC
Type
Human Prescription Drug
Product code
0006-0227

Recalls naming this package

Class II ยท Moderate risk

Raltegravir

Labeling: Label Mixup: RALTEGRAVIR, Tablet, 400 mg may be potentially mis-labeled as one of the following drugs: HYDROCORTISONE, Tablet, 5 mg, NDC00603389919, Pedigree: AD60272_13, EXP: 5/22/2014; HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg, NDC 00574025001, Pedigree: W003679, EXP: 6/25/2014; HYDROCORTISONE, Tablet, 5 mg, NDC 00603389919, Pedigree: AD21790_16, EXP: 5/1/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-775-2014

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