Active Ingredient: AMILORIDE HYDROCHLORIDE
Proprietary Name: AMILORIDE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A204180
Product Number: 001
Approval Date: Aug 7, 2015
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
