Active Ingredient: BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE
Proprietary Name: KERLEDEX
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG;12.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019807
Product Number: 002
Approval Date: Oct 30, 1992
Applicant Holder Full Name: SANOFI AVENTIS US LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
