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

Is NDC 65862-0638-30 recalled?

Irbesartan · 30 TABLET in 1 BOTTLE (65862-638-30)

Yes — this exact package was recalled

1 FDA recall names the code 65862-0638-30 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
Irbesartan
Strength
IRBESARTAN 150 mg/1
Form
Tablet · Oral
Labeler
Aurobindo Pharma Limited
Type
Human Prescription Drug
Product code
65862-0638

Recalls naming this package

Class II ยท Moderate risk

Irbesartan

Labeling:Label Mixup; IRBESARTAN, Tablet, 150 mg may be potentially mislabeled as ATROPINE SULFATE/DIPHENOXYLATE HCL, Tablet, 0.025 mg/2.5 mg, NDC 00378041501, Pedigree: W003597, EXP: 6/24/2014; CHOLECALCIFEROL, Tablet, 400 units, NDC 00904582360, Pedigree: AD76686_7, EXP: 5/31/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-717-2014

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