General MedicationsTOPICALGeneric

NUTRACORT

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1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 NUTRACORT is listed in Drugs@FDA under application 084698 (ANDA).

Marketing status: Discontinued Active ingredient HYDROCORTISONE Form and strength GEL;TOPICAL - 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor HEALTHPOINT Submission history Latest submission status date: 1992-03-13 00:00:00.

Structured Monograph

Clinical summary

Approval overview NUTRACORT is listed in Drugs@FDA under application 084698 (ANDA). Marketing status: Discontinued Active ingredient HYDROCORTISONE Form and strength GEL;TOPICAL - 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor HEALTHPOINT Submission history Latest submission status date: 1992-03-13 00:00:00. Submission type: SUPPL.

Monitoring

• Marketing status: Discontinued

Interaction Notes

No interaction notes stored yet.