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General MedicationsTOPICALGeneric

PRAMOSONE

HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

Standard Dose
0.5%;1%
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview PRAMOSONE is listed in Drugs@FDA under application 083213 (ANDA).

Marketing status: Discontinued Active ingredient HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE Form and strength LOTION;TOPICAL - 0.5%;1% Sponsor FERNDALE LABS Submission history Latest submission status date: 1973-11-13 00:00:00.

Structured Monograph

Clinical summary

Approval overview PRAMOSONE is listed in Drugs@FDA under application 083213 (ANDA). Marketing status: Discontinued Active ingredient HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE Form and strength LOTION;TOPICAL - 0.5%;1% Sponsor FERNDALE LABS Submission history Latest submission status date: 1973-11-13 00:00:00. Submission type: ORIG.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.