Norepinephrine Bitartrate 47335-0615
Product NDC
47335-0615- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 1, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA211980
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Norepinephrine Bitartrate | 1 mg/mL |
Drug Class
Catecholamine [EPC]Catecholamines [CS]
Packaging Options(1)
10 VIAL, SINGLE-DOSE in 1 CARTON (47335-615-44) / 4 mL in 1 VIAL, SINGLE-DOSE