NDC 45963-304
dextroamphetamine sulfate 10 mg capsule, extended release
On the label: Actavis Pharma, Inc..
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
- Jul 11, 2016 · Class II · Actavis Inc
Failed Dissolution Specifications
Lots: Lot #: 3803J141, Exp. 7/2016
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Dextroamphetamine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA203901
- On the market since
- Jun 19, 2014
- Package NDCs
45963-304-09- Official label
- DailyMed (National Library of Medicine), updated Apr 13, 2026
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