Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated May 22, 2020 (6 years ago)

Dextroamphetamine Saccharate

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Some bottles may contain mixed strengths of the product.

Cause type: Labeling / mix-up

Wrong label, wrong strength, mixed-up products, or packaging errors. One of the most dangerous causes - you can end up taking the wrong drug or the wrong dose. All labeling / mix-up recalls.

What was recalled

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets ( Mixed Amphetamine Salts Product), 5 mg, 100 count bottles, Rx Only, Teva Pharmaceuticals USA, INC. North Wales, PA 19454, NDC 0555-0971-02

Affected NDC 0555-0971-02

Compare with the code on your package — it is the most precise check available.

Drug: Dextroamphetamine

Product details

From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.

ProductStrengthForm & routeLabelerType
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate
NDC 00555-0971
DEXTROAMPHETAMINE SACCHARATE 1.25 mg/1; AMPHETAMINE ASPARTATE MONOHYDRATE 1.25 mg/1; DEXTROAMPHETAMINE SULFATE 1.25 mg/1; AMPHETAMINE SULFATE 1.25 mg/1 Tablet
Oral
Teva Pharmaceuticals USA, Inc. Rx · CII
Recalling firm
Teva Pharmaceuticals USA
NDC code
0555-0971-02
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1285-2020 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Dextroamphetamine recalls

See all
Class II · Moderate risk

Dextroamphetamine Saccharate

Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.

Ongoing Labeling / mix-up Lannett Company Inc. D-0660-2026

Other recalls by Teva Pharmaceuticals USA

All 2020 recalls