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General MedicationsORALGeneric

MICRO-K LS

POTASSIUM CHLORIDE

Standard Dose
20MEQ/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview MICRO-K LS is listed in Drugs@FDA under application 019561 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient POTASSIUM CHLORIDE Form and strength FOR SUSPENSION, EXTENDED RELEASE;ORAL - 20MEQ/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor KV PHARM Submission history Latest submission status date: 2005-08-22 00:00:00.

Structured Monograph

Clinical summary

Approval overview MICRO-K LS is listed in Drugs@FDA under application 019561 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient POTASSIUM CHLORIDE Form and strength FOR SUSPENSION, EXTENDED RELEASE;ORAL - 20MEQ/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor KV PHARM Submission history Latest submission status date: 2005-08-22 00:00:00. Submission type: SUPPL.

Monitoring

  • Marketing status: Discontinued
  • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.
MICRO-K LS (POTASSIUM CHLORIDE) | Drug Monograph | MedicHelpline