Alprazolam
- Product NDC
- 72789-313
- 11-digit product format
- 727890313
- Labeler code
- 72789
- Product ID
- 72789-313_40bb1fd8-e70f-47eb-e063-6394a90a74a8
- 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
- .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 |
|---|
| 72789-313-06 | 72789031306 | 6 TABLET in 1 BOTTLE, PLASTIC (72789-313-06) | 6 tablet | 2024-06-18 | No | No | Historical |
| 72789-313-30 | 72789031330 | 30 TABLET in 1 BOTTLE, PLASTIC (72789-313-30) | 30 tablet | 2023-07-31 | No | No | Historical |
| 72789-313-60 | 72789031360 | 60 TABLET in 1 BOTTLE, PLASTIC (72789-313-60) | 60 tablet | 2023-05-09 | No | No | Historical |
| 72789-313-90 | 72789031390 | 90 TABLET in 1 BOTTLE, PLASTIC (72789-313-90) | 90 tablet | 2023-03-16 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam | PD-Rx Pharmaceuticals, Inc. | 2025-10-09 | HUMAN PRESCRIPTION DRUG LABEL | 21 |
| Alprazolam | PD-Rx Pharmaceuticals, Inc. | 2024-06-18 | HUMAN PRESCRIPTION DRUG LABEL | 20 |