Alprazolam
- Product NDC
- 72789-328
- 11-digit product format
- 727890328
- Labeler code
- 72789
- Product ID
- 72789-328_40bb38f6-3141-72c2-e063-6294a90a2a78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA074342
- Marketing category
- ANDA
- Marketing start
- 1993-10-01
- 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 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-328-30 | Alprazolam | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 20 |
| 72789-328-60 | Alprazolam | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | | 20 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-328 | ALPRAZOLAM TABLET [PD-RX PHARMACEUTICALS, INC.] | 19 | Current NDC, 2 package rows | 20241011_2f16ff78-1262-4bb8-9a25-822c13c4746f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72789-328-30 | 72789032830 | 30 TABLET in 1 BOTTLE, PLASTIC (72789-328-30) | 30 tablet | 2023-06-12 | No | No | Current |
| 72789-328-60 | 72789032860 | 60 TABLET in 1 BOTTLE, PLASTIC (72789-328-60) | 60 tablet | 2023-06-12 | No | No | Current |