Class II · Moderate risk
Dextroamphetamine Saccharate
Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.
National Drug Code
Is NDC 0527-0790-37 recalled?
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate · 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-0790-37)
Yes — this exact package was recalled
1 FDA recall names the code 0527-0790-37 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.
1 of these recalls is still ongoing.
- Active ingredient
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amphetamine Sulfate and Amphetamine Aspartate
- Strength
- DEXTROAMPHETAMINE SULFATE 1.25 mg/1; DEXTROAMPHETAMINE…
- Form
- Capsule, Extended Release · Oral
- Labeler
- Lannett Company, Inc.
- Type
- Human Prescription Drug · DEA CII
- Product code
- 0527-0790
Recalls naming this package
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
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