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General MedicationsTOPICALStandard

PRAMOSONE

HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

Standard Dose
2.5%;1%
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Prescription
Summary

Approval overview PRAMOSONE is listed in Drugs@FDA under application 085979 (ANDA).

Marketing status: Prescription Active ingredient HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE Form and strength LOTION;TOPICAL - 2.5%;1% Sponsor LEGACY PHARMA Submission history Latest submission status date: 2002-01-24 00:00:00.

Structured Monograph

Clinical summary

Approval overview PRAMOSONE is listed in Drugs@FDA under application 085979 (ANDA). Marketing status: Prescription Active ingredient HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE Form and strength LOTION;TOPICAL - 2.5%;1% Sponsor LEGACY PHARMA Submission history Latest submission status date: 2002-01-24 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Prescription

Interaction Notes

  • No interaction notes stored yet.