Amphetamine Sulfate
- Product NDC
- 50742-651
- 11-digit product format
- 507420651
- Labeler code
- 50742
- Product ID
- 50742-651_c9e9fd46-5480-4054-9039-3cd9f5eb8aa1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amphetamine Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA213763
- Marketing category
- ANDA
- Marketing start
- 2020-08-24
- Marketing end
- 0000-00-00
- Substance
- AMPHETAMINE 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50742-651-01 | 50742065101 | 100 TABLET in 1 BOTTLE (50742-651-01) | 100 tablet | 2020-08-24 | 0000-00-00 | No | No | Current |