Dextroamphetamine SulfateExtended-Release
- Product NDC
- 0115-1702
- 11-digit product format
- 001151702
- Labeler code
- 0115
- Product ID
- 0115-1702_27072364-bca1-4260-bffe-29e409573f4f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dextroamphetamine Sulfate
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Application
- NDA017078
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1976-08-02
- Marketing end
- 0000-00-00
- Substance
- DEXTROAMPHETAMINE SULFATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0115-1702-10 | 00115170210 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0115-1702-10) | 1976-08-02 | 0000-00-00 | No | No | Current |