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General MedicationsINJECTIONGeneric

AMIKACIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

AMIKACIN SULFATE

Standard Dose
EQ 500MG BASE/100ML
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview AMIKACIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER is listed in Drugs@FDA under application 064146 (ANDA).

Marketing status: Discontinued Active ingredient AMIKACIN SULFATE Form and strength INJECTABLE;INJECTION - EQ 500MG BASE/100ML Sponsor HOSPIRA Submission history Latest submission status date: 1999-02-22 00:00:00.

Structured Monograph

Clinical summary

Approval overview AMIKACIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER is listed in Drugs@FDA under application 064146 (ANDA). Marketing status: Discontinued Active ingredient AMIKACIN SULFATE Form and strength INJECTABLE;INJECTION - EQ 500MG BASE/100ML Sponsor HOSPIRA Submission history Latest submission status date: 1999-02-22 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.