FdaApplication
ANDA 080235
Identifiers
- fda_app_no: ANDA080235
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | ANDA |
| approval_date | 1983-03-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VASOCON | NAPHAZOLINE HYDROCHLORIDE | 0.1% | SOLUTION/DROPS;OPHTHALMIC |
1 product