Alprazolam
- Product NDC
- 68071-3818
- 11-digit product format
- 680713818
- Labeler code
- 68071
- Product ID
- 68071-3818_315b8d50-f3b5-49a4-e063-6394a90ae849
- 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
- .5 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 |
|---|
| 68071-3818-1 | 68071381801 | 1000 TABLET in 1 BOTTLE (68071-3818-1) | 1000 tablet | 2025-03-27 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam | NuCare Pharmaceuticals, Inc. | 2025-03-27 | HUMAN PRESCRIPTION DRUG LABEL | 1 |