Active Ingredient: ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE
Proprietary Name: FOAMICON
Dosage Form; Route of Administration: TABLET, CHEWABLE; ORAL
Strength: 80MG;20MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A072687
Product Number: 001
Approval Date: Jun 28, 1989
Applicant Holder Full Name: NOVARTIS CONSUMER HEALTH INC
Marketing Status:
Discontinued
Patent and Exclusivity Information