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: Yes
TE Code: AB
Application Number: A073209
Product Number: 001
Approval Date: Oct 31, 1991
Applicant Holder Full Name: RISING PHARMA HOLDING INC
Marketing Status:
Prescription
Patent and Exclusivity Information
