AMPHETAMINE SULFATE
- Product NDC
- 71337-025
- 11-digit product format
- 713370025
- Labeler code
- 71337
- Product ID
- 71337-025_6c7f2ea6-a673-4e70-9a39-6067057fe6d7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMPHETAMINE SULFATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Havix Group Inc d-b-a Aavis Pharmaceuticals
- Application
- ANDA212901
- Marketing category
- ANDA
- Marketing start
- 2020-10-22
- Marketing end
- 0000-00-00
- Substance
- AMPHETAMINE 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71337-025-01 | 71337002501 | 100 TABLET in 1 BOTTLE (71337-025-01) | 100 tablet | 2020-10-23 | 0000-00-00 | No | No | Current |