Dextroamphetamine Saccharate — Class II drug recall D-1490-2016
Terminated recall by Amerisource Health Services, reported 2016-09-14, distributed nationwide. Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
| Recall number | D-1490-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Amerisource Health Services, Columbus, OH, United States |
| Recall initiated | 2016-08-24 |
| Classified | 2016-09-02 |
| Reported by FDA | 2016-09-14 |
| Terminated | 2017-12-18 |
| Distributed | Nationwide (US) |
| Quantity | 761 cartons |
| NDC | 68084-0887-32, 68084-0887-33 |
| Lot numbers | 152418, 153544, 154835 |
| Expiration dates | 2016-12-31, 2017-03-31, 2017-05-31 |
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 30 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 68084-887-32; Blister NDC 68084-887-33
Reason for recall
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
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-1490-2016. 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.