FdaApplication
ANDA 072687
Identifiers
- fda_app_no: ANDA072687
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS CONSUMER HEALTH INC |
| application_type | ANDA |
| approval_date | 1989-06-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FOAMICON | ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE | 80MG;20MG | TABLET, CHEWABLE;ORAL |
1 product