Betapace AF
- Product NDC
- 13672-056
- 11-digit product format
- 136720056
- Labeler code
- 13672
- Product ID
- 13672-056_d723021a-3258-876b-e053-2995a90a3e77
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sotalol HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Skyepharma Production SAS
- Application
- NDA021151
- Marketing category
- NDA
- Marketing start
- 2000-02-22
- Marketing end
- 0000-00-00
- Substance
- SOTALOL HYDROCHLORIDE
- Active strength
- 160 mg/160mg
- 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 |
|---|
| 13672-056-00 | 13672005600 | 60 mg in 1 BOTTLE (13672-056-00) | 60 mg | 2000-02-22 | 0000-00-00 | No | No | Current |