Diazepam 68071-4770
Product NDC
68071-4770- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- December 10, 1986
- Listing Expires
- December 31, 2026
- Application
- ANDA071321
Active Ingredients
| Ingredient | Strength |
|---|---|
| Diazepam | 5 mg/1 |
Drug Class
Benzodiazepine [EPC]Benzodiazepine [EPC]Benzodiazepines [CS]
Packaging Options(4)
10 TABLET in 1 BOTTLE (68071-4770-1)
30 TABLET in 1 BOTTLE (68071-4770-3)
15 TABLET in 1 BOTTLE (68071-4770-5)
90 TABLET in 1 BOTTLE (68071-4770-9)