Alprazolam
- Product NDC
- 71610-696
- 11-digit product format
- 716100696
- Labeler code
- 71610
- Product ID
- 71610-696_f27967d7-9517-4c95-81a2-29408e707f5a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA074112
- Marketing category
- ANDA
- Marketing start
- 1995-12-29
- Substance
- ALPRAZOLAM
- Active strength
- .25 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 71610-696-15 | 71610069615 | 15 TABLET in 1 BOTTLE (71610-696-15) | 15 tablet | 2023-03-20 | No | No | Historical |
| 71610-696-30 | 71610069630 | 30 TABLET in 1 BOTTLE (71610-696-30) | 30 tablet | 2023-03-20 | No | No | Historical |
| 71610-696-45 | 71610069645 | 45 TABLET in 1 BOTTLE (71610-696-45) | 45 tablet | 2023-03-20 | No | No | Historical |
| 71610-696-53 | 71610069653 | 60 TABLET in 1 BOTTLE (71610-696-53) | 60 tablet | 2023-03-20 | No | No | Historical |
| 71610-696-60 | 71610069660 | 90 TABLET in 1 BOTTLE (71610-696-60) | 90 tablet | 2023-03-20 | No | No | Historical |
| 71610-696-70 | 71610069670 | 120 TABLET in 1 BOTTLE (71610-696-70) | 120 tablet | 2023-03-20 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam | Aphena Pharma Solutions - Tennessee, LLC | 2023-03-20 | HUMAN PRESCRIPTION DRUG LABEL | 1 |