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

Is NDC 68462-0390-30 recalled?

Esomeprazole Magnesium · 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (68462-390-30)

Yes — this exact package was recalled

1 FDA recall names the code 68462-0390-30 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
Esomeprazole Magnesium
Strength
ESOMEPRAZOLE MAGNESIUM 20 mg/1
Form
Capsule, Delayed Release Pellets · Oral
Labeler
Glenmark Pharmaceuticals Inc., USA
Type
Human Prescription Drug
Product code
68462-0390

Recalls naming this package

Class III · Low risk

Esomeprazole Magnesium Delayed-Release Capsules

Failed Impurities/Degradation Specifications:Out of Specification result reported for the test of organic impurities for the drug product,at the 18 month time point in long term stability study (25¿C/60% RH).

Terminated Impurity / degradation Glenmark Pharmaceuticals Inc., USA NDC 68462-390-30 D-0112-2024

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