General MedicationsTOPICALGeneric
LOCOID
HYDROCORTISONE BUTYRATE
Standard Dose
0.1%
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary
Approval overview LOCOID is listed in Drugs@FDA under application 019819 (NDA).
Marketing status: Discontinued Active ingredient HYDROCORTISONE BUTYRATE Form and strength SOLUTION;TOPICAL - 0.1% Sponsor YAMANOUCHI Submission history See approval history documents.
Structured Monograph
Clinical summary
Approval overview LOCOID is listed in Drugs@FDA under application 019819 (NDA). Marketing status: Discontinued Active ingredient HYDROCORTISONE BUTYRATE Form and strength SOLUTION;TOPICAL - 0.1% Sponsor YAMANOUCHI Submission history See approval history documents.
Monitoring
- • Marketing status: Discontinued
Interaction Notes
- No interaction notes stored yet.