FdaApplication
ANDA 062341
Identifiers
- fda_app_no: ANDA062341
Properties
| Property | Value |
|---|---|
| applicant_name | SANDOZ INC |
| application_type | ANDA |
| approval_date | 1984-05-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MAXITROL | DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE | 0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML | SUSPENSION/DROPS;OPHTHALMIC |
1 product