Diazepam 68682-0652
Product NDC
68682-0652- Manufacturer
- Oceanside Pharmaceuticals
- Dosage Form
- Gel
- Route
- Rectal
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- July 29, 1997
- Listing Expires
- December 31, 2026
- Application
- NDA020648
Active Ingredients
| Ingredient | Strength |
|---|---|
| Diazepam | 10 mg/2mL |
Drug Class
Benzodiazepine [EPC]Benzodiazepine [EPC]Benzodiazepines [CS]
Packaging Options(1)
2 SYRINGE, PLASTIC in 1 PACKAGE (68682-652-20) / 2 mL in 1 SYRINGE, PLASTIC