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

Is NDC 0054-0021-25 recalled?

Lithium Carbonate · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0021-25)

Yes — this exact package was recalled

1 FDA recall names the code 0054-0021-25 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
Lithium Carbonate
Strength
LITHIUM CARBONATE 300 mg/1
Form
Tablet, Extended Release · Oral
Labeler
Hikma Pharmaceuticals USA Inc.
Type
Human Prescription Drug
Product code
0054-0021

Recalls naming this package

Class II · Moderate risk

Lithium Carbonate ER

Labeling: Label Mixup: LITHIUM CARBONATE ER, Tablet, 300 mg may be potentially mislabled as the following drug: VITAMIN B COMPLEX PROLONGED RELEASE, Tablet, 50 mg, NDC 40985022251, Pedigree: AD39588_10, EXP: 5/13/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-791-2014

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