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

Is NDC 0527-0762-37 recalled?

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate · 100 TABLET in 1 BOTTLE (0527-0762-37)

Yes — this exact package was recalled

1 FDA recall names the code 0527-0762-37 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
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate
Strength
DEXTROAMPHETAMINE SACCHARATE 2.5 mg/1; AMPHETAMINE…
Form
Tablet · Oral
Labeler
Lannett Company, LLC
Type
Human Prescription Drug · DEA CII
Product code
0527-0762

Recalls naming this package

Class II · Moderate risk

Dextroamphetamine Saccharate

Presence of Foreign Tablet/Capsule: Two (2) bottles labeled as Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 10mg, 100ct, contained one (1) tablet of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 5 mg.

Completed Particulate / foreign matter Lannett Company Inc. NDC 0527-0762-37 D-0642-2025

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