ALPRAZOLAM
- Product NDC
- 61919-849
- 11-digit product format
- 619190849
- Labeler code
- 61919
- Product ID
- 61919-849_94dee553-82b9-0d0f-e053-2995a90a2843
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALPRAZOLAM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA074174
- Marketing category
- ANDA
- Marketing start
- 2019-09-18
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-849-30 | ALPRAZOLAM | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 61919-849-60 | ALPRAZOLAM | 60 in 1 BOTTLE | TABLET | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-849 | ALPRAZOLAM TABLET [DIRECT_RX] | 2 | Legacy NDC, 2 package rows | 20191015_92d435d1-aef5-d28f-e053-2a95a90a9eda.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 |
|---|
| 61919-849-30 | 61919084930 | 30 TABLET in 1 BOTTLE (61919-849-30) | 30 tablet | 2019-09-18 | 0000-00-00 | No | No | Current |
| 61919-849-60 | 61919084960 | 60 TABLET in 1 BOTTLE (61919-849-60) | 60 tablet | 2019-09-18 | 0000-00-00 | No | No | Current |