Ephedrine Sulfate 00781-3269
Product NDC
00781-3269- Manufacturer
- Sandoz Inc
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- October 1, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA209784
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ephedrine Sulfate | 50 mg/mL |
Drug Class
Adrenergic alpha-Agonists [MoA]Adrenergic beta-Agonists [MoA]Increased Norepinephrine Activity [PE]
Packaging Options(1)
10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3269-95) / 1 mL in 1 VIAL, SINGLE-DOSE (0781-3269-71)