Nicardipine Hydrochloride 70069-0876
Product NDC
70069-0876- Manufacturer
- Somerset Therapeutics, Llc
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- April 20, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA220243
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Nicardipine Hydrochloride | .2 mg/mL |
Drug Class
Calcium Channel Antagonists [MoA]Cytochrome P450 2C19 Inhibitors [MoA]Cytochrome P450 2C8 Inhibitors [MoA]
Packaging Options(1)
10 POUCH in 1 CASE (70069-876-10) / 1 BAG in 1 POUCH (70069-876-01) / 200 mL in 1 BAG