FdaApplication
ANDA 062521
Identifiers
- fda_app_no: ANDA062521
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1985-07-11 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OTOCORT | HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE | 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML | SUSPENSION/DROPS;OTIC |
1 product