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General MedicationsINJECTIONGeneric

MEFOXIN IN PLASTIC CONTAINER

CEFOXITIN SODIUM

Standard Dose
EQ 20MG BASE/ML
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview MEFOXIN IN PLASTIC CONTAINER is listed in Drugs@FDA under application 063182 (ANDA).

Marketing status: Discontinued Active ingredient CEFOXITIN SODIUM Form and strength INJECTABLE;INJECTION - EQ 20MG BASE/ML Sponsor PHARMOBEDIENT Submission history Latest submission status date: 2017-03-07 00:00:00.

Structured Monograph

Clinical summary

Approval overview MEFOXIN IN PLASTIC CONTAINER is listed in Drugs@FDA under application 063182 (ANDA). Marketing status: Discontinued Active ingredient CEFOXITIN SODIUM Form and strength INJECTABLE;INJECTION - EQ 20MG BASE/ML Sponsor PHARMOBEDIENT Submission history Latest submission status date: 2017-03-07 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.