Alprazolam
- Product NDC
- 80425-0099
- 11-digit product format
- 804250099
- Labeler code
- 80425
- Product ID
- 80425-0099_2a994e77-4ae4-1307-e063-6394a90a5bd3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Advanced Rx of Tennessee, LLC
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Alprazolam
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALPRAZOLAM | .5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YU55MQ3IZY |
| Rxcui | 308048 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80425-0099-2 | Alprazolam | 60 in 1 BOTTLE | TABLET | 60 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80425-0099 | ALPRAZOLAM TABLET [ADVANCED RX OF TENNESSEE, LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250101_b39e2bc8-b68f-0f4e-e053-2995a90a00fd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80425-0099-2 | 80425009902 | 60 TABLET in 1 BOTTLE (80425-0099-2) | 60 tablet | 1993-10-01 | 0000-00-00 | No | No | Current |