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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.
CEFUROXIME SODIUM (CEFUROXIME SODIUM) | Drug Monograph | MedicHelpline