Active Ingredient: AMILORIDE HYDROCHLORIDE
Proprietary Name: MIDAMOR
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N018200
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PADAGIS US LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
