Active Ingredient: HYDROCHLOROTHIAZIDE; METHYLDOPA
Proprietary Name: METHYLDOPA AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG;250MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A070366
Product Number: 001
Approval Date: Apr 16, 1986
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information