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General MedicationsINJECTIONGeneric

MANDOL

CEFAMANDOLE NAFATE

Standard Dose
EQ 500MG BASE/VIAL
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview MANDOL is listed in Drugs@FDA under application 050504 (NDA).

Marketing status: Discontinued Active ingredient CEFAMANDOLE NAFATE Form and strength INJECTABLE;INJECTION - EQ 500MG BASE/VIAL Sponsor LILLY Submission history Latest submission status date: 2009-03-13 00:00:00.

Structured Monograph

Clinical summary

Approval overview MANDOL is listed in Drugs@FDA under application 050504 (NDA). Marketing status: Discontinued Active ingredient CEFAMANDOLE NAFATE Form and strength INJECTABLE;INJECTION - EQ 500MG BASE/VIAL Sponsor LILLY 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.
MANDOL (CEFAMANDOLE NAFATE) | Drug Monograph | MedicHelpline