Alprazolam
- Product NDC
- 51991-704
- 11-digit product format
- 519910704
- Labeler code
- 51991
- Product ID
- 51991-704_94163352-f78e-400a-b7da-b3075e9213eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Application
- ANDA207507
- Marketing category
- ANDA
- Marketing start
- 2018-07-09
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 0 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51991-704 | ALPRAZOLAM TABLET [BRECKENRIDGE PHARMACEUTICAL, INC.] | 6 | Legacy NDC | 20230728_67f66894-addc-4e92-855a-c9ae03a5c2c5.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 |
|---|
| 51991-704-01 | 51991070401 | 100 TABLET in 1 BOTTLE (51991-704-01) | 100 tablet | 2018-07-09 | 0000-00-00 | No | No | Current |
| 51991-704-05 | 51991070405 | 500 TABLET in 1 BOTTLE (51991-704-05) | 500 tablet | 2018-07-09 | 0000-00-00 | No | No | Current |
| 51991-704-10 | 51991070410 | 1000 TABLET in 1 BOTTLE (51991-704-10) | 1000 tablet | 2018-07-09 | 0000-00-00 | No | No | Current |