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General MedicationsTOPICALGeneric

DERMATOP E EMOLLIENT

PREDNICARBATE

Standard Dose
0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 DERMATOP E EMOLLIENT is listed in Drugs@FDA under application 020279 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient PREDNICARBATE Form and strength CREAM;TOPICAL - 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VALEANT BERMUDA Submission history Latest submission status date: 2010-12-06 00:00:00.

Structured Monograph

Clinical summary

Approval overview DERMATOP E EMOLLIENT is listed in Drugs@FDA under application 020279 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient PREDNICARBATE Form and strength CREAM;TOPICAL - 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VALEANT BERMUDA Submission history Latest submission status date: 2010-12-06 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.
DERMATOP E EMOLLIENT (PREDNICARBATE) | Drug Monograph | MedicHelpline