FdaApplication
ANDA 075219
Identifiers
- fda_app_no: ANDA075219
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 1998-08-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM | 50MG | TABLET;ORAL |
1 product