Alprazolam
- Product NDC
- 71205-227
- 11-digit product format
- 712050227
- Labeler code
- 71205
- Product ID
- 71205-227_c256eb0e-ff92-498d-9a9d-820b63126233
- 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
- 2023-12-31
- 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 |
|---|
| 71205-227 | ALPRAZOLAM TABLET [PROFICIENT RX LP] | 6 | Legacy NDC | 20221116_2d04c305-70d6-4a99-8c82-720c5398a46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-227-10 | 71205022710 | 10 TABLET in 1 BOTTLE (71205-227-10) | 10 tablet | 2022-11-10 | 0000-00-00 | No | No | Current |
| 71205-227-30 | 71205022730 | 30 TABLET in 1 BOTTLE (71205-227-30) | 30 tablet | 2019-02-01 | 0000-00-00 | No | No | Current |
| 71205-227-60 | 71205022760 | 60 TABLET in 1 BOTTLE (71205-227-60) | 60 tablet | 2019-02-01 | 0000-00-00 | No | No | Current |
| 71205-227-90 | 71205022790 | 90 TABLET in 1 BOTTLE (71205-227-90) | 90 tablet | 2019-02-01 | 0000-00-00 | No | No | Current |