Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate 57664-0950
Product NDC
57664-0950- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- February 1, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA215997
Active Ingredients
| Ingredient | Strength |
|---|---|
| Amphetamine Aspartate Monohydrate | 3.125 mg/1 |
| Amphetamine Sulfate | 3.125 mg/1 |
| Dextroamphetamine Saccharate | 3.125 mg/1 |
| Dextroamphetamine Sulfate | 3.125 mg/1 |
Drug Class
Central Nervous System Stimulant [EPC]Central Nervous System Stimulant [EPC]Central Nervous System Stimulant [EPC]
Packaging Options(1)
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (57664-950-88)