Alprazolam
- Product NDC
- 68788-7613
- 11-digit product format
- 687887613
- Labeler code
- 68788
- Product ID
- 68788-7613_81283b2e-86a4-418b-8f12-8d918b0ce059
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA207507
- Marketing category
- ANDA
- Marketing start
- 2020-02-07
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 2 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7613-2 | 68788761302 | 20 TABLET in 1 BOTTLE (68788-7613-2) | 20 tablet | 2020-02-07 | 0000-00-00 | No | No | Current |
| 68788-7613-3 | 68788761303 | 30 TABLET in 1 BOTTLE (68788-7613-3) | 30 tablet | 2020-02-07 | 0000-00-00 | No | No | Current |
| 68788-7613-6 | 68788761306 | 60 TABLET in 1 BOTTLE (68788-7613-6) | 60 tablet | 2020-02-07 | 0000-00-00 | No | No | Current |
| 68788-7613-9 | 68788761309 | 90 TABLET in 1 BOTTLE (68788-7613-9) | 90 tablet | 2020-02-07 | 0000-00-00 | No | No | Current |