Sotalol Hydrochloride 69724-0112
Product NDC
69724-0112- Manufacturer
- Altathera Pharmaceuticals, Llc
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- October 15, 2015
- Listing Expires
- December 31, 2026
- Application
- NDA022306
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sotalol Hydrochloride | 15 mg/mL |
Drug Class
Adrenergic beta-Antagonists [MoA]Antiarrhythmic [EPC]Cardiac Rhythm Alteration [PE]
Packaging Options(1)
1 VIAL in 1 CARTON (69724-112-10) / 10 mL in 1 VIAL