General MedicationsINJECTIONGeneric

PRIMACOR IN DEXTROSE 5% IN PLASTIC CONTAINER

MILRINONE LACTATE

Standard Dose

EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 PRIMACOR IN DEXTROSE 5% IN PLASTIC CONTAINER is listed in Drugs@FDA under application 020343 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient MILRINONE LACTATE Form and strength INJECTABLE;INJECTION - EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SANOFI AVENTIS US Submission history Latest submission status date: 2007-10-30 00:00:00.

Structured Monograph

Clinical summary

Approval overview PRIMACOR IN DEXTROSE 5% IN PLASTIC CONTAINER is listed in Drugs@FDA under application 020343 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient MILRINONE LACTATE Form and strength INJECTABLE;INJECTION - EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SANOFI AVENTIS US Submission history Latest submission status date: 2007-10-30 00:00:00. Submission type: SUPPL.

Monitoring

• Marketing status: Discontinued
• Review priority: STANDARD

Interaction Notes

No interaction notes stored yet.