Alprazolam
- Product NDC
- 49999-032
- 11-digit product format
- 499990032
- Labeler code
- 49999
- Product ID
- 49999-032_af362455-d7c9-4ce2-81b1-30d4dfdfe10b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALPRAZOLAM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA074112
- Marketing category
- ANDA
- Marketing start
- 2010-04-01
- 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
- 2022-12-31
- 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 |
|---|
| 49999-032-30 | 49999003230 | 30 TABLET in 1 BOTTLE, PLASTIC (49999-032-30) | 30 tablet | 2010-04-01 | 0000-00-00 | No | No | Current |
| 49999-032-60 | 49999003260 | 60 TABLET in 1 BOTTLE, PLASTIC (49999-032-60) | 60 tablet | 2010-04-01 | 0000-00-00 | No | No | Current |
| 49999-032-90 | 49999003290 | 90 TABLET in 1 BOTTLE, PLASTIC (49999-032-90) | 90 tablet | 2010-04-01 | 0000-00-00 | No | No | Current |