NDC 68382-950
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate 4 ingredients tablet
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Nesher Pharmaceuticals (USA) LLC | Location not on file | Makes it and tests it | Not inspected on record |
Product details
- Generic drug
- Amphetamine and Dextroamphetamine: every company that makes it
- Form
- tablet
- Strength
- 4 ingredients
- Approval
- ANDA ANDA207340
- On the market since
- Oct 31, 2017
- Package NDCs
68382-950-01- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2020
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