FdaApplication
NDA 018746
Identifiers
- fda_app_no: NDA018746
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1994-07-11 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VASOCON-A | ANTAZOLINE PHOSPHATE; NAPHAZOLINE HYDROCHLORIDE | 0.5%;0.05% | SOLUTION/DROPS;OPHTHALMIC |
1 product