DEXTROAMPHETAMINE SULFATE
- Product NDC
- 63629-2374
- 11-digit product format
- 636292374
- Labeler code
- 63629
- Product ID
- 63629-2374_b5518c08-44f3-46b8-bbd5-217f441baf3b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dextroamphetamine sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210059
- Marketing category
- ANDA
- Marketing start
- 2018-07-04
- 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 |
|---|
| 63629-2374-1 | 63629237401 | 100 TABLET in 1 BOTTLE (63629-2374-1) | 100 tablet | 2018-07-04 | No | No | Historical |