FdaApplication
ANDA 073508
Identifiers
- fda_app_no: ANDA073508
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS PHARMA INC AN INDIRECT WHOLLY OWNED SUB OF TEVA PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 1993-11-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MICONAZOLE NITRATE | MICONAZOLE NITRATE | 200MG | SUPPOSITORY;VAGINAL |
1 product