Diazepam 68071-3682
Product NDC
68071-3682- Manufacturer
- Nucare Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- December 14, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA217843
Active Ingredients
| Ingredient | Strength |
|---|---|
| Diazepam | 5 mg/1 |
Drug Class
Benzodiazepine [EPC]Benzodiazepine [EPC]Benzodiazepines [CS]
Packaging Options(2)
10 TABLET in 1 BOTTLE (68071-3682-1)
6 TABLET in 1 BOTTLE (68071-3682-6)