Active Ingredient: HYDROCHLOROTHIAZIDE
Proprietary Name: HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 50MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A089661
Product Number: 001
Approval Date: Jun 20, 1988
Applicant Holder Full Name: MORTON GROVE PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
