Alprazolam 68071-2220
Product NDC
68071-2220- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- October 1, 1993
- Listing Expires
- December 31, 2026
- Application
- ANDA074342
Active Ingredients
| Ingredient | Strength |
|---|---|
| Alprazolam | .5 mg/1 |
Drug Class
Benzodiazepine [EPC]Benzodiazepine [EPC]Benzodiazepines [CS]
Packaging Options(1)
30 TABLET in 1 BOTTLE (68071-2220-3)