Xanax
- Product NDC
- 58151-452
- 11-digit product format
- 581510452
- Labeler code
- 58151
- Product ID
- 58151-452_27062ff4-9ce3-4d8a-aeae-f4468efb623a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Viatris Specialty LLC
- Application
- NDA018276
- Marketing category
- NDA
- Marketing start
- 2025-10-29
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Xanax
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALPRAZOLAM | .25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YU55MQ3IZY |
| Rxcui | 141927, 141928, 197321, 197322, 214003, 214004, 308047, 308048 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58151-452-01 | Xanax | 100 in 1 BOTTLE | TABLET | 100 | | 4 |
| 58151-452-05 | Xanax | 500 in 1 BOTTLE | TABLET | 500 | | 4 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 58151-452-01 | 58151045201 | 100 TABLET in 1 BOTTLE (58151-452-01) | 100 tablet | 2025-10-29 | No | No | Current |
| 58151-452-05 | 58151045205 | 500 TABLET in 1 BOTTLE (58151-452-05) | 500 tablet | 2025-10-29 | No | No | Current |