Alprazolam
- Product NDC
- 67296-1379
- 11-digit product format
- 672961379
- Labeler code
- 67296
- Product ID
- 67296-1379_9c9f9369-30a5-3cec-e053-2a95a90a8cef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA200739
- Marketing category
- ANDA
- Marketing start
- 2015-10-01
- 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
- 2021-12-31
- 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 |
|---|
| 67296-1379-2 | Alprazolam | 20 in 1 BOTTLE | TABLET | 20 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1379 | ALPRAZOLAM TABLET [REDPHARM DRUG, INC.] | 2 | Legacy NDC, 1 package rows | 20200121_504ba5ad-0a50-4f85-e054-00144ff88e88.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 |
|---|
| 67296-1379-2 | 67296137902 | 20 TABLET in 1 BOTTLE (67296-1379-2) | 20 tablet | 2015-10-01 | 0000-00-00 | No | No | Current |