NDC 0527-0761
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate 4 ingredients tablet
On the label: Lannett Company, 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 Lannett Company, Inc. names for other drugs.
Recalls
- Aug 19, 2025 · Class II · Lannett Company Inc.
Presence of Foreign Tablet/Capsule: Two (2) bottles labeled as Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 10mg, 100ct, contained one (1) tablet of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 5 mg.
Lots: Lot#: 25283185A. Expiry: 02/28/2027
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
- tablet, oral
- Strength
- 4 ingredients
- Approval
- ANDA ANDA215565
- On the market since
- Jul 8, 2022
- Package NDCs
0527-0761-37- Official label
- DailyMed (National Library of Medicine), updated Jul 21, 2026
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