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CardiovascularORALGeneric

PRAVASTATIN SODIUM

PRAVASTATIN SODIUM

Standard Dose
30MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview PRAVASTATIN SODIUM is listed in Drugs@FDA under application 077730 (ANDA).

Marketing status: Discontinued Active ingredient PRAVASTATIN SODIUM Form and strength TABLET;ORAL - 30MG Sponsor PLIVA HRVATSKA DOO Submission history Latest submission status date: 2006-11-21 00:00:00.

Structured Monograph

Clinical summary

Approval overview PRAVASTATIN SODIUM is listed in Drugs@FDA under application 077730 (ANDA). Marketing status: Discontinued Active ingredient PRAVASTATIN SODIUM Form and strength TABLET;ORAL - 30MG Sponsor PLIVA HRVATSKA DOO Submission history Latest submission status date: 2006-11-21 00:00:00. Submission type: ORIG.

Monitoring

  • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.