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General MedicationsTOPICALGeneric

HYDROCORTISONE ACETATE 1% AND PRAMOXINE HYDROCHLORIDE 1%

HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

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

Approval overview HYDROCORTISONE ACETATE 1% AND PRAMOXINE HYDROCHLORIDE 1% is listed in Drugs@FDA under application 089440 (ANDA).

Marketing status: Discontinued Active ingredient HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE Form and strength AEROSOL, METERED;TOPICAL - 1%;1% Sponsor GENUS Submission history Latest submission status date: 2000-08-11 00:00:00.

Structured Monograph

Clinical summary

Approval overview HYDROCORTISONE ACETATE 1% AND PRAMOXINE HYDROCHLORIDE 1% is listed in Drugs@FDA under application 089440 (ANDA). Marketing status: Discontinued Active ingredient HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE Form and strength AEROSOL, METERED;TOPICAL - 1%;1% Sponsor GENUS Submission history Latest submission status date: 2000-08-11 00:00:00. Submission type: SUPPL.

Monitoring

  • • Review priority: UNKNOWN
  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.