Alprazolam 59762-3719
Product NDC
59762-3719- Manufacturer
- Mylan Pharmaceuticals Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- October 16, 1981
- Listing Expires
- December 31, 2026
- Application
- NDA018276
Active Ingredients
| Ingredient | Strength |
|---|---|
| Alprazolam | .25 mg/1 |
Drug Class
Benzodiazepine [EPC]Benzodiazepine [EPC]Benzodiazepines [CS]
Packaging Options(3)
100 TABLET in 1 BOTTLE (59762-3719-1)
500 TABLET in 1 BOTTLE (59762-3719-3)
1000 TABLET in 1 BOTTLE (59762-3719-4)