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FOAMICON

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: NOVARTIS · Approved 1989-06-28

Drug application

FDA Application #

ANDA072687

Application type

Abbreviated New Drug Application (Generic)

Brand name

FOAMICON

Generic name

Aluminum Hydroxide

Active ingredients

ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE

Dosage form

TABLET, CHEWABLE

Route

ORAL

Marketing status

Discontinued

Sponsor

NOVARTIS

First approval

1989-06-28

Source

Authoritative

Drugs@FDA application overview

Machine

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