FdaApplication
NDA 020805
Identifiers
- fda_app_no: NDA020805
Properties
| Property | Value |
|---|---|
| applicant_name | SANDOZ INC |
| application_type | NDA |
| approval_date | 1998-02-10 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CIPRO HC | CIPROFLOXACIN HYDROCHLORIDE; HYDROCORTISONE | EQ 0.2% BASE;1% | SUSPENSION/DROPS;OTIC |
1 product