NOVANTRONE
MITOXANTRONE HYDROCHLORIDE
Approval overview NOVANTRONE is listed in Drugs@FDA under application 019297 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient MITOXANTRONE HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - EQ 20MG BASE/10ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor EMD SERONO Submission history Latest submission status date: 2012-03-23 00:00:00.
Structured Monograph
Clinical summary
Approval overview NOVANTRONE is listed in Drugs@FDA under application 019297 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient MITOXANTRONE HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - EQ 20MG BASE/10ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor EMD SERONO Submission history Latest submission status date: 2012-03-23 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.