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General MedicationsORALGeneric

LUDIOMIL

MAPROTILINE HYDROCHLORIDE

Standard Dose
50MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview LUDIOMIL is listed in Drugs@FDA under application 017543 (NDA).

Marketing status: Discontinued Active ingredient MAPROTILINE HYDROCHLORIDE Form and strength TABLET;ORAL - 50MG Sponsor NOVARTIS Submission history Latest submission status date: 1997-04-10 00:00:00.

Structured Monograph

Clinical summary

Approval overview LUDIOMIL is listed in Drugs@FDA under application 017543 (NDA). Marketing status: Discontinued Active ingredient MAPROTILINE HYDROCHLORIDE Form and strength TABLET;ORAL - 50MG Sponsor NOVARTIS Submission history Latest submission status date: 1997-04-10 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.