Sodium Bicarbonate 70095-0050
Product NDC
70095-0050- Manufacturer
- Sun Pharmaceutical Industries Limited
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- March 15, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA217594
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sodium Bicarbonate | 84 mg/mL |
Drug Class
Alkalinizing Activity [MoA]
Packaging Options(1)
25 VIAL in 1 CARTON (70095-050-03) / 50 mL in 1 VIAL (70095-050-01)