Alprazolam
- Product NDC
- 50090-2256
- 11-digit product format
- 500902256
- Labeler code
- 50090
- Product ID
- 50090-2256_97516c92-6bf3-42a8-ae1d-eff880f72b62
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074174
- Marketing category
- ANDA
- Marketing start
- 2007-03-28
- 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
- 2021-12-31
- 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 |
|---|
| 50090-2256-0 | 50090225600 | 30 TABLET in 1 BOTTLE (50090-2256-0) | 30 tablet | 2015-12-07 | 0000-00-00 | No | No | Current |
| 50090-2256-4 | 50090225604 | 90 TABLET in 1 BOTTLE (50090-2256-4) | 90 tablet | 2015-12-07 | 0000-00-00 | No | No | Current |