Alprazolam
- Product NDC
- 68788-7577
- 11-digit product format
- 687887577
- Labeler code
- 68788
- Product ID
- 68788-7577_370c6726-6201-42b3-9366-885ca160e65a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA074342
- Marketing category
- ANDA
- Marketing start
- 1993-10-01
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 0 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| YU55MQ3IZY | ALPRAZOLAM | 28981-97-7 | ALPRAZOLAM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7577-2 | 68788757702 | 20 TABLET in 1 BOTTLE (68788-7577-2) | 20 tablet | 2019-10-31 | 0000-00-00 | No | No | Current |
| 68788-7577-3 | 68788757703 | 30 TABLET in 1 BOTTLE (68788-7577-3) | 30 tablet | 2019-10-31 | 0000-00-00 | No | No | Current |
| 68788-7577-6 | 68788757706 | 60 TABLET in 1 BOTTLE (68788-7577-6) | 60 tablet | 2019-10-31 | 0000-00-00 | No | No | Current |
| 68788-7577-9 | 68788757709 | 90 TABLET in 1 BOTTLE (68788-7577-9) | 90 tablet | 2019-10-31 | 0000-00-00 | No | No | Current |