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General MedicationsTOPICALGeneric

ALPHADERM

HYDROCORTISONE; UREA

Standard Dose
1%;10%
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview ALPHADERM is listed in Drugs@FDA under application 086008 (ANDA).

Marketing status: Discontinued Active ingredient HYDROCORTISONE; UREA Form and strength CREAM;TOPICAL - 1%;10% Sponsor BIOGLAN Submission history Latest submission status date: 1987-10-19 00:00:00.

Structured Monograph

Clinical summary

Approval overview ALPHADERM is listed in Drugs@FDA under application 086008 (ANDA). Marketing status: Discontinued Active ingredient HYDROCORTISONE; UREA Form and strength CREAM;TOPICAL - 1%;10% Sponsor BIOGLAN Submission history Latest submission status date: 1987-10-19 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.