NDC 13107-072
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate 4 ingredients tablet
On the label: Aurolife Pharma LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
Recalls
- Sep 19, 2019 · Class II · Aurobindo Pharma USA Inc.
Superpotent Drug: Amphetamine Mixed Salts 20mg have been found to be out of specification for weight and thickness.
Lots: Batch 07319032A1, Exp 02/2021
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 ANDA202424
- On the market since
- Nov 27, 2013
- Package NDCs
13107-072-0113107-072-0513107-072-2513107-072-5013107-072-99- Official label
- DailyMed (National Library of Medicine), updated Jul 31, 2026
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