FdaApplication
NDA 018988
Identifiers
- fda_app_no: NDA018988
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1988-08-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VASOCIDIN | PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM | EQ 0.23% PHOSPHATE;10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SOLUTION/DROPS;OPHTHALMIC |
1 product