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General MedicationsORALGeneric

GRIFULVIN V

GRISEOFULVIN, MICROSIZE

Standard Dose
125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview GRIFULVIN V is listed in Drugs@FDA under application 062483 (ANDA).

Marketing status: Discontinued Active ingredient GRISEOFULVIN, MICROSIZE Form and strength SUSPENSION;ORAL - 125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VALEANT LUXEMBOURG Submission history Latest submission status date: 2015-11-02 00:00:00.

Structured Monograph

Clinical summary

Approval overview GRIFULVIN V is listed in Drugs@FDA under application 062483 (ANDA). Marketing status: Discontinued Active ingredient GRISEOFULVIN, MICROSIZE Form and strength SUSPENSION;ORAL - 125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VALEANT LUXEMBOURG Submission history Latest submission status date: 2015-11-02 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.