FdaApplication
ANDA 075345
Identifiers
- fda_app_no: ANDA075345
Properties
| Property | Value |
|---|---|
| applicant_name | IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA |
| application_type | ANDA |
| approval_date | 1999-06-16 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CIMETIDINE | CIMETIDINE | 200MG | TABLET;ORAL |
1 product