Alprazolam
- Product NDC
- 49999-039
- 11-digit product format
- 499990039
- Labeler code
- 49999
- Product ID
- 49999-039_189cc961-c8a8-4706-8768-e1db58056c92
- 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
- 0 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| YU55MQ3IZY | ALPRAZOLAM | 28981-97-7 | ALPRAZOLAM |