Active Ingredient: AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Proprietary Name: AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 5MG ANHYDROUS;50MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A073357
Product Number: 001
Approval Date: Nov 27, 1991
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
