FdaApplication
NDA 018685
Identifiers
- fda_app_no: NDA018685
Properties
| Property | Value |
|---|---|
| applicant_name | CHATTEM INC DBA SANOFI CONSUMER HEALTHCARE |
| application_type | NDA |
| approval_date | 1983-12-09 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| GAVISCON | ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE | 160MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, CHEWABLE;ORAL |
| GAVISCON | ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE | 80MG;20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, CHEWABLE;ORAL |
2 products