General MedicationsTOPICALGeneric

HYTONE

HYDROCORTISONE

Standard Dose

1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Max Dose

Refer to approved labeling

Primary Use

Marketing status: Discontinued

Summary

Approval overview HYTONE is listed in Drugs@FDA under application 080473 (ANDA).

Marketing status: Discontinued Active ingredient HYDROCORTISONE Form and strength LOTION;TOPICAL - 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VALEANT INTL Submission history Latest submission status date: 2002-03-27 00:00:00.

Structured Monograph

Clinical summary

Approval overview HYTONE is listed in Drugs@FDA under application 080473 (ANDA). Marketing status: Discontinued Active ingredient HYDROCORTISONE Form and strength LOTION;TOPICAL - 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VALEANT INTL Submission history Latest submission status date: 2002-03-27 00:00:00. Submission type: SUPPL.

Monitoring

• Marketing status: Discontinued

Interaction Notes

No interaction notes stored yet.