FdaApplication
NDA 050749
Identifiers
- fda_app_no: NDA050749
Properties
| Property | Value |
|---|---|
| applicant_name | ABBVIE INC |
| application_type | NDA |
| approval_date | 1997-12-04 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OMNICEF | CEFDINIR | 125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | FOR SUSPENSION;ORAL |
| OMNICEF | CEFDINIR | 250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | FOR SUSPENSION;ORAL |
2 products