Details for New Drug Application (NDA): 072687

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NDA 072687 describes FOAMICON, which is a drug marketed by Novartis and is included in one NDA. Additional details are available on the FOAMICON profile page.

The generic ingredient in FOAMICON is aluminum hydroxide; magnesium trisilicate. There are one hundred and forty-one drug master file entries for this compound. Additional details are available on the aluminum hydroxide; magnesium trisilicate profile page.

Summary for 072687

Tradename:	FOAMICON
Applicant:	Novartis
Ingredient:	aluminum hydroxide; magnesium trisilicate
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET, CHEWABLE;ORAL			Strength	80MG;20MG
Approval Date:	Jun 28, 1989	TE:		RLD:	No

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