FdaApplication
ANDA 076699
Identifiers
- fda_app_no: ANDA076699
Properties
| Property | Value |
|---|---|
| applicant_name | UCB INC |
| application_type | ANDA |
| approval_date | 2004-08-27 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PARCOPA | CARBIDOPA; LEVODOPA | 25MG;250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, ORALLY DISINTEGRATING;ORAL |
| PARCOPA | CARBIDOPA; LEVODOPA | 10MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, ORALLY DISINTEGRATING;ORAL |
| PARCOPA | CARBIDOPA; LEVODOPA | 25MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, ORALLY DISINTEGRATING;ORAL |
3 products