Active Ingredient: HYDROCHLOROTHIAZIDE; METHYLDOPA
Proprietary Name: METHYLDOPA AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG;500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071461
Product Number: 001
Approval Date: Mar 8, 1988
Applicant Holder Full Name: IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:
Discontinued
Patent and Exclusivity Information
