FdaApplication
ANDA 076736
Identifiers
- fda_app_no: ANDA076736
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA FARMACEUTICA PORTUGAL LDA |
| application_type | ANDA |
| approval_date | 2005-08-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FLUCONAZOLE IN SODIUM CHLORIDE 0.9% | FLUCONAZOLE | 200MG/100ML (2MG/ML) | INJECTABLE;INJECTION |
1 product