FdaApplication
ANDA 086156
Identifiers
- fda_app_no: ANDA086156
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NITROFURAZONE | NITROFURAZONE | 0.2% | OINTMENT;TOPICAL |
1 product