Dextroamphetamine Sulfate
- Product NDC
- 72162-2350
- 11-digit product format
- 721622350
- Labeler code
- 72162
- Product ID
- 72162-2350_9dd752c2-6687-4190-a3b5-ca2c1c6a0ba4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dextroamphetamine Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090533
- Marketing category
- ANDA
- Marketing start
- 2012-07-20
- Substance
- DEXTROAMPHETAMINE SULFATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| JJ768O327N | DEXTROAMPHETAMINE SULFATE | 51-63-8 | DEXTROAMPHETAMINE SULFATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2350-3 | 72162235003 | 30 TABLET in 1 BOTTLE (72162-2350-3) | 30 tablet | 2021-04-14 | No | No | Historical |