Alprazolam
- Product NDC
- 50090-1864
- 11-digit product format
- 500901864
- Labeler code
- 50090
- Product ID
- 50090-1864_71cb1809-575a-436e-be2f-2a457cd1a17d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074112
- Marketing category
- ANDA
- Marketing start
- 1995-12-29
- Marketing end
- 2027-03-19
- Substance
- ALPRAZOLAM
- Active strength
- .25 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| YU55MQ3IZY | ALPRAZOLAM | 28981-97-7 | ALPRAZOLAM |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam | A-S Medication Solutions | 2025-07-10 | HUMAN PRESCRIPTION DRUG LABEL | 27 |