Dextroamphetamine Sulfate
- Product NDC
- 72162-2353
- 11-digit product format
- 721622353
- Labeler code
- 72162
- Product ID
- 72162-2353_ce15c3db-cae3-4697-9bcc-20d3ba949d4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dextroamphetamine Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090533
- Marketing category
- ANDA
- Marketing start
- 2021-08-06
- Substance
- DEXTROAMPHETAMINE SULFATE
- Active strength
- 30 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 |
|---|
| 72162-2353-3 | 72162235303 | 30 TABLET in 1 BOTTLE (72162-2353-3) | 30 tablet | 2024-08-14 | No | No | Historical |