Active Ingredient: HYDROCHLOROTHIAZIDE; METHYLDOPA
Proprietary Name: METHYLDOPA AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 15MG;250MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071897
Product Number: 001
Approval Date: Nov 23, 1987
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:
Discontinued
Patent and Exclusivity Information