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General MedicationsINJECTIONGeneric

DAUNORUBICIN HYDROCHLORIDE

DAUNORUBICIN HYDROCHLORIDE

Standard Dose
EQ 5MG BASE/VIAL
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview DAUNORUBICIN HYDROCHLORIDE is listed in Drugs@FDA under application 065034 (ANDA).

Marketing status: Discontinued Active ingredient DAUNORUBICIN HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - EQ 5MG BASE/VIAL Sponsor FRESENIUS KABI USA Submission history Latest submission status date: 2002-06-18 00:00:00.

Structured Monograph

Clinical summary

Approval overview DAUNORUBICIN HYDROCHLORIDE is listed in Drugs@FDA under application 065034 (ANDA). Marketing status: Discontinued Active ingredient DAUNORUBICIN HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - EQ 5MG BASE/VIAL Sponsor FRESENIUS KABI USA Submission history Latest submission status date: 2002-06-18 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.