Sotalol Hydrochloride
- Product NDC
- 71335-0860
- 11-digit product format
- 713350860
- Labeler code
- 71335
- Product ID
- 71335-0860_806090ef-a698-416b-a79c-24265e1f2c51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sotalol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075429
- Marketing category
- ANDA
- Marketing start
- 2000-05-04
- Marketing end
- 0000-00-00
- Substance
- SOTALOL HYDROCHLORIDE
- Active strength
- 80 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0860-1 | 71335086001 | 60 TABLET in 1 BOTTLE (71335-0860-1) | 60 tablet | 2018-06-13 | 0000-00-00 | No | No | Current |
| 71335-0860-2 | 71335086002 | 30 TABLET in 1 BOTTLE (71335-0860-2) | 30 tablet | 2018-06-13 | 0000-00-00 | No | No | Current |
| 71335-0860-3 | 71335086003 | 100 TABLET in 1 BOTTLE (71335-0860-3) | 100 tablet | 2018-06-13 | 0000-00-00 | No | No | Current |