High Outlier
Strength
5 mg/mL
Manufacturer
Azurity Pharmaceuticals Inc.NDC
24338053048
Classification
Brand
Dosage Form
SOLUTION
Route
ORAL
Last Updated
1/1/2026
Active Ingredients
SOTALOL HYDROCHLORIDEApproval Type
New Drug (NDA)
FDA Application
NDA205108On Market Since
3/1/2015
Pharmacological Classes
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