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General MedicationsTOPICALGeneric

AMCINONIDE

AMCINONIDE

Standard Dose
0.1%
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview AMCINONIDE is listed in Drugs@FDA under application 076367 (ANDA).

Marketing status: Discontinued Active ingredient AMCINONIDE Form and strength OINTMENT;TOPICAL - 0.1% Sponsor TARO PHARM INDS Submission history Latest submission status date: 2003-03-19 00:00:00.

Structured Monograph

Clinical summary

Approval overview AMCINONIDE is listed in Drugs@FDA under application 076367 (ANDA). Marketing status: Discontinued Active ingredient AMCINONIDE Form and strength OINTMENT;TOPICAL - 0.1% Sponsor TARO PHARM INDS Submission history Latest submission status date: 2003-03-19 00:00:00. Submission type: ORIG.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.