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General MedicationsINJECTIONGeneric

RUBEX

DOXORUBICIN HYDROCHLORIDE

Standard Dose
100MG/VIAL
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview RUBEX is listed in Drugs@FDA under application 062926 (ANDA).

Marketing status: Discontinued Active ingredient DOXORUBICIN HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - 100MG/VIAL Sponsor BRISTOL MYERS SQUIBB Submission history Latest submission status date: 2001-05-24 00:00:00.

Structured Monograph

Clinical summary

Approval overview RUBEX is listed in Drugs@FDA under application 062926 (ANDA). Marketing status: Discontinued Active ingredient DOXORUBICIN HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - 100MG/VIAL Sponsor BRISTOL MYERS SQUIBB Submission history Latest submission status date: 2001-05-24 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.