Alprazolam
- Product NDC
- 63629-2942
- 11-digit product format
- 636292942
- Labeler code
- 63629
- Product ID
- 63629-2942_c89986aa-e7a2-46ed-9df5-784a1bd7e09d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074342
- Marketing category
- ANDA
- Marketing start
- 2008-04-02
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| YU55MQ3IZY | ALPRAZOLAM | 28981-97-7 | ALPRAZOLAM |