Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, 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 Actavis Pharma, Inc. names for other drugs.

Recalls

• Feb 13, 2013 · Class III · Actavis Elizabeth LLC
  Failed Dissolution Specification: This product recall is due to the product lot # 50077231 exceeding dissolution specifications. All other test specifications were met.
  Lots: Lot #: 50077231

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 ANDA077302

On the market since

Jun 22, 2012

Package NDCs

0228-3060-11

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?