FdaApplication
ANDA 088791
Identifiers
- fda_app_no: ANDA088791
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | ANDA |
| approval_date | 1984-10-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VASOCIDIN | PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM | 0.5%;10% | OINTMENT;OPHTHALMIC |
1 product