Dextroamphetamine Saccharate — Class II drug recall D-0642-2025
Completed recall by Lannett Company Inc., reported 2025-09-17, distributed in OH. Presence of Foreign Tablet/Capsule: Two (2) bottles labeled as Dextroamphetamine Saccharate, Amphetamine Aspar
| Recall number | D-0642-2025 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lannett Company Inc., Seymour, IN, United States |
| Recall initiated | 2025-08-19 |
| Classified | 2025-09-11 |
| Reported by FDA | 2025-09-17 |
| Distributed | OH |
| Quantity | 4,848 bottles |
| Reason classes | labeling |
| NDC | 00527-0760, 00527-0760-37, 00527-0761, 00527-0761-37, 00527-0762, 00527-0762-37, 00527-0763, 00527-0763-37, 00527-0764, 00527-0764-37, 00527-0765, 00527-0765-37, 00527-0766, 00527-0766-37 |
| Lot numbers | 25283185A |
| Expiration dates | 2027-02-28 |
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 10mg, 100 Tablets per bottle, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-0762-37.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0642-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.