Sotalol Hydrochloride
- Product NDC
- 70518-3341
- 11-digit product format
- 705183341
- Labeler code
- 70518
- Product ID
- 70518-3341_d80e4625-6878-0e07-e053-2a95a90a9626
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sotalol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076140
- Marketing category
- ANDA
- Marketing start
- 2022-01-24
- Marketing end
- 0000-00-00
- Substance
- SOTALOL HYDROCHLORIDE
- Active strength
- 120 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], Antiarrhythmic [EPC], Cardiac Rhythm Alteration [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| HEC37C70XX | SOTALOL HYDROCHLORIDE | 959-24-0 | SOTALOL HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3341-0 | 70518334100 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3341-0) | 90 tablet | 2022-01-24 | 0000-00-00 | No | No | Current |