Alprazolam
- Product NDC
- 71205-284
- 11-digit product format
- 712050284
- Labeler code
- 71205
- Product ID
- 71205-284_4e3e8db2-3859-41b6-a5a2-e460ba65b9e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA207507
- Marketing category
- ANDA
- Marketing start
- 2018-07-09
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-284 | ALPRAZOLAM TABLET [PROFICIENT RX LP] | 4 | Legacy NDC | 20230115_7732dbd7-96b4-49ea-8984-7a5b0e554bfd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-284-30 | 71205028430 | 30 TABLET in 1 BOTTLE (71205-284-30) | 30 tablet | 2019-06-01 | 0000-00-00 | No | No | Current |
| 71205-284-60 | 71205028460 | 60 TABLET in 1 BOTTLE (71205-284-60) | 60 tablet | 2019-06-01 | 0000-00-00 | No | No | Current |
| 71205-284-90 | 71205028490 | 90 TABLET in 1 BOTTLE (71205-284-90) | 90 tablet | 2019-06-01 | 0000-00-00 | No | No | Current |