FdaApplication
NDA 050581
Identifiers
- fda_app_no: NDA050581
Properties
| Property | Value |
|---|---|
| applicant_name | MERCK AND CO INC |
| application_type | NDA |
| approval_date | 1984-09-20 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | CEFOXITIN SODIUM | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | CEFOXITIN SODIUM | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | CEFOXITIN SODIUM | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | CEFOXITIN SODIUM | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
4 products