Sotalol Hydrochloride 72789-0135
Product NDC
72789-0135- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 24, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA075563
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sotalol Hydrochloride | 160 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]Antiarrhythmic [EPC]Cardiac Rhythm Alteration [PE]
Packaging Options(1)
100 TABLET in 1 BOTTLE, PLASTIC (72789-135-01)