Sotalol Hydrochloride 00904-7143
Product NDC
00904-7143- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 1, 2003
- Listing Expires
- December 31, 2026
- Application
- ANDA076140
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sotalol Hydrochloride | 80 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]Antiarrhythmic [EPC]Cardiac Rhythm Alteration [PE]
Packaging Options(1)
100 BLISTER PACK in 1 CARTON (0904-7143-61) / 1 TABLET in 1 BLISTER PACK