Alprazolam
- Product NDC
- 50268-035
- 11-digit product format
- 502680035
- Labeler code
- 50268
- Product ID
- 50268-035_3fa15074-b724-8144-e063-6294a90a5c84
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA203346
- Marketing category
- ANDA
- Marketing start
- 2025-08-25
- Substance
- ALPRAZOLAM
- Active strength
- 1 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
- Alprazolam
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALPRAZOLAM | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YU55MQ3IZY |
| Rxcui | 197321, 308047, 308048 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50268-035-11 | Alprazolam | 1 in 1 BLISTER PACK | TABLET | 1 | | 1 |
| 50268-035-15 | Alprazolam | 50 in 1 BOX | TABLET | 50 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50268-035-11 | 50268003511 | 1 in 1 BLISTER PACK | | | | | Historical |
| 50268-035-15 | 50268003515 | 50 BLISTER PACK in 1 BOX (50268-035-15) / 1 TABLET in 1 BLISTER PACK (50268-035-11) | 50 blister pack | 2025-08-25 | No | No | Current |