FdaApplication
ANDA 062501
Identifiers
- fda_app_no: ANDA062501
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | ANDA |
| approval_date | 1984-07-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| GENTACIDIN | GENTAMICIN SULFATE | EQ 0.3% BASE | OINTMENT;OPHTHALMIC |
1 product