Alprazolam
- Product NDC
- 68071-2976
- 11-digit product format
- 680712976
- Labeler code
- 68071
- Product ID
- 68071-2976_137bc7a0-62bd-f5e1-e063-6294a90a0dcb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA203346
- Marketing category
- ANDA
- Marketing start
- 2015-07-31
- Substance
- ALPRAZOLAM
- Active strength
- 2 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 |
|---|
| 68071-2976-9 | 68071297609 | 90 TABLET in 1 BOTTLE (68071-2976-9) | 90 tablet | 2023-04-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam | NuCare Pharmaceuticals,Inc. | 2024-03-12 | HUMAN PRESCRIPTION DRUG LABEL | 3 |