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General MedicationsINJECTIONGeneric

PLASMA-LYTE 56 IN PLASTIC CONTAINER

MAGNESIUM ACETATE TETRAHYDRATE; POTASSIUM ACETATE; SODIUM CHLORIDE

Standard Dose
32MG/100ML;128MG/100ML;234MG/100ML
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview PLASMA-LYTE 56 IN PLASTIC CONTAINER is listed in Drugs@FDA under application 019047 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient MAGNESIUM ACETATE TETRAHYDRATE; POTASSIUM ACETATE; SODIUM CHLORIDE Form and strength INJECTABLE;INJECTION - 32MG/100ML;128MG/100ML;234MG/100ML Sponsor BAXTER HLTHCARE Submission history Latest submission status date: 2005-08-24 00:00:00.

Structured Monograph

Clinical summary

Approval overview PLASMA-LYTE 56 IN PLASTIC CONTAINER is listed in Drugs@FDA under application 019047 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient MAGNESIUM ACETATE TETRAHYDRATE; POTASSIUM ACETATE; SODIUM CHLORIDE Form and strength INJECTABLE;INJECTION - 32MG/100ML;128MG/100ML;234MG/100ML Sponsor BAXTER HLTHCARE Submission history Latest submission status date: 2005-08-24 00:00:00. Submission type: SUPPL.

Monitoring

  • Marketing status: Discontinued
  • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.
PLASMA-LYTE 56 IN PLASTIC CONTAINER (MAGNESIUM ACETATE TETRAHYDRATE; POTASSIUM ACETATE; SODIUM CHLORIDE) | Drug Monograph | MedicHelpline