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General MedicationsINJECTIONGeneric

VASCORAY

IOTHALAMATE MEGLUMINE; IOTHALAMATE SODIUM

Standard Dose
52%;26%
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview VASCORAY is listed in Drugs@FDA under application 016783 (NDA).

Marketing status: Discontinued Active ingredient IOTHALAMATE MEGLUMINE; IOTHALAMATE SODIUM Form and strength INJECTABLE;INJECTION - 52%;26% Sponsor MALLINCKRODT Submission history Latest submission status date: 2009-03-13 00:00:00.

Structured Monograph

Clinical summary

Approval overview VASCORAY is listed in Drugs@FDA under application 016783 (NDA). Marketing status: Discontinued Active ingredient IOTHALAMATE MEGLUMINE; IOTHALAMATE SODIUM Form and strength INJECTABLE;INJECTION - 52%;26% Sponsor MALLINCKRODT Submission history Latest submission status date: 2009-03-13 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.