FdaApplication
ANDA 075910
Identifiers
- fda_app_no: ANDA075910
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS ELIZABETH LLC |
| application_type | ANDA |
| approval_date | 2002-01-07 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | 100MG | TABLET, EXTENDED RELEASE;ORAL |
1 product