General MedicationsINTRAMUSCULAR, INTRAVENOUSGeneric
CEFUROXIME SODIUM
CEFUROXIME SODIUM
Standard Dose
EQ 750MG BASE/VIAL
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary
Approval overview CEFUROXIME SODIUM is listed in Drugs@FDA under application 065483 (ANDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient CEFUROXIME SODIUM Form and strength INJECTABLE;INTRAMUSCULAR, INTRAVENOUS - EQ 750MG BASE/VIAL Sponsor HOSPIRA INC Submission history Latest submission status date: 2016-04-12 00:00:00.
Structured Monograph
Clinical summary
Approval overview CEFUROXIME SODIUM is listed in Drugs@FDA under application 065483 (ANDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient CEFUROXIME SODIUM Form and strength INJECTABLE;INTRAMUSCULAR, INTRAVENOUS - EQ 750MG BASE/VIAL Sponsor HOSPIRA INC Submission history Latest submission status date: 2016-04-12 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.