Esomeprazole Sodium 70436-0190
Product NDC
70436-0190- Manufacturer
- Slate Run Pharmaceuticals, Llc
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- February 25, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA215732
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Esomeprazole Sodium | 40 mg/5mL |
Drug Class
Cytochrome P450 2C19 Inhibitors [MoA]Proton Pump Inhibitor [EPC]Proton Pump Inhibitors [MoA]
Packaging Options(1)
10 VIAL in 1 CARTON (70436-190-82) / 5 mL in 1 VIAL (70436-190-80)