Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate 4 ingredients capsule, extended release

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Lannett Company, Inc. names for other drugs.

Recalls

• Jun 26, 2026 · Class II · Lannett Company Inc.
  Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.
  Lots: Lot#: 25285401A, Exp. Date: 04/2027

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Amphetamine and Dextroamphetamine: every company that makes it

Form

capsule, extended release, oral

Strength

4 ingredients

Approval

ANDA ANDA214403

On the market since

Nov 26, 2021

Package NDCs

0527-0792-37

Official label

DailyMed (National Library of Medicine), updated May 1, 2026

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?