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Betapace Online, Description, Chemistry, Ingredients - Sotalol Hydrochloride
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To minimize the risk of induced arrhythmia, patients initiated or re-initiated onBETAPACE AFTM should be placed for a minimum of three days (on their maintenance dose) in a facility that can provide cardiac resuscitation, continuous electrocardiographic monitoring and calculations of creatinine clearance. For detailed instructions regarding dose selection and special cautions for people with renal impairment, see DOSAGE AND ADMINISTRATION. Sotalol is also indicated for the treatment of documented life-threatening ventricular arrhythmias and is marketed under the brand name BETAPACETM. BETAPACE however, must not should not be substituted for BETAPACE AFTM because of significant differences in labeling (i.e. patient package insert, dosing administration and safety information). |
DESCRIPTION
BETAPACE AFTM, (sotalol hydrochloride), is an antiarrhythmic drug with Class II (beta-adrenoreceptor blocking) and Class III (cardiac action potential duration prolongation) properties. It is supplied as a white, capsule-shaped tablet for oral administration. Sotalol hydrochloride is a white, crystalline solid with a molecular weight of 308.8. It is hydrophilic, soluble in water, propylene glycol and ethanol, but is only slightly soluble in chloroform. Chemically, sotalol hydrochloride is d,l-N-[4-[l-hydroxy-2-[(l-methylethyl) amino]ethyl]phenyl]methane-sulfonamide monohydrochloride. The molecular formula is
C12H20N2O3S·HCl
BETAPACE AFTM tablets contain the following inactive ingredients: microcrystalline cellulose, lactose, starch, stearic acid, magnesium stearate, and colloidal silicon dioxide.
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