Active Ingredient: HYDROCHLOROTHIAZIDE
Proprietary Name: HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A087539
Product Number: 001
Approval Date: Feb 3, 1982
Applicant Holder Full Name: ASCOT HOSP PHARMACEUTICALS INC DIV TRAVENOL LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information