# FOAMICON
> **ANDA072687** · Abbreviated New Drug Application (Generic) · Sponsor: NOVARTIS · Approved 1989-06-28
## Drug
- **FDA Application Number:** 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
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=072687)
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