BETAPACE AF 80 mg/1
sotalol hydrochloride · TABLET · Legacy Pharma USA, Inc.
No Recall History
Plain English
BETAPACE AF is a tablet containing sotalol hydrochloride at 80 mg/1, taken oral. Manufactured by Legacy Pharma USA, Inc..
Key Facts
- Brand Name
- BETAPACE AF
- Generic Name
- sotalol hydrochloride
- NDC Code (Product)
83107-008- Manufacturer
- Legacy Pharma USA, Inc.
- Strength
- 80 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- NDA019865
- Marketing Start
- 09/01/2016
Recall History
No Recall HistoryFrequently Asked Questions
What is BETAPACE AF used for?
BETAPACE AF contains sotalol hydrochloride. It is a tablet taken oral. Consult your doctor for specific uses.
Is BETAPACE AF a controlled substance?
BETAPACE AF is not classified as a controlled substance by the DEA.
What is the generic name for BETAPACE AF?
The generic name for BETAPACE AF is sotalol hydrochloride. There are 12 other brand versions of sotalol hydrochloride.
What is the NDC code for BETAPACE AF 80 mg/1?
The NDC (National Drug Code) for BETAPACE AF 80 mg/1 is 83107-008, listed by Legacy Pharma USA, Inc..
Other Sotalol Brands
See all →- Sotalol80 mg/172162-2524
- Sotalol Hydrochloride80 mg/172789-137
- BETAPACE160 mg/183107-007
- Sotalol Hydrochloride80 mg/10904-7143
- Sotalol Hydrochloride80 mg/150090-1299
- Sotalol80 mg/171335-1189
- Sotalol Hydrochloride80 mg/171610-474
- Sotalol Hydrochloride240 mg/172789-136
- Sotalol Hydrochloride120 mg/172789-138
- Sotalol80 mg/176385-114
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)