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.