Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate
- Product NDC
- 72162-2054
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211352
- Marketing category
- ANDA
- Substance
- AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-2054-1 | 100 TABLET in 1 BOTTLE (72162-2054-1) | 2023-06-14 | | No | Historical |
| 72162-2054-3 | 30 TABLET in 1 BOTTLE (72162-2054-3) | 2023-06-14 | | No | Historical |
| 72162-2054-6 | 60 TABLET in 1 BOTTLE (72162-2054-6) | 2023-06-14 | | No | Historical |
| 72162-2054-9 | 90 TABLET in 1 BOTTLE (72162-2054-9) | 2023-06-14 | | No | Historical |