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General MedicationsTOPICALGeneric

NAFTIN

NAFTIFINE HYDROCHLORIDE

Standard Dose
1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 NAFTIN is listed in Drugs@FDA under application 019599 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient NAFTIFINE HYDROCHLORIDE Form and strength CREAM;TOPICAL - 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor LEGACY PHARMA Submission history Latest submission status date: 2018-04-30 00:00:00.

Structured Monograph

Clinical summary

Approval overview NAFTIN is listed in Drugs@FDA under application 019599 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient NAFTIFINE HYDROCHLORIDE Form and strength CREAM;TOPICAL - 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor LEGACY PHARMA Submission history Latest submission status date: 2018-04-30 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.