Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 050581
Company: MERCK
Company: MERCK
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
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CONTAINER | CEFOXITIN SODIUM | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION | Discontinued | None | Yes | No |
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CONTAINER | CEFOXITIN SODIUM | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION | Discontinued | None | Yes | No |
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CONTAINER | CEFOXITIN SODIUM | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION | Discontinued | None | Yes | No |
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CONTAINER | CEFOXITIN SODIUM | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION | Discontinued | None | Yes | No |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
02/27/1997 | SUPPL-20 |
Review
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/nda/97/50-517s031_50-581s020_Mefoxin.cfm |