CORLOPAM
FENOLDOPAM MESYLATE
Approval overview CORLOPAM is listed in Drugs@FDA under application 019922 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient FENOLDOPAM MESYLATE Form and strength INJECTABLE;INJECTION - EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor HOSPIRA Submission history Latest submission status date: 2020-09-02 00:00:00.
Structured Monograph
Clinical summary
Approval overview CORLOPAM is listed in Drugs@FDA under application 019922 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient FENOLDOPAM MESYLATE Form and strength INJECTABLE;INJECTION - EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor HOSPIRA Submission history Latest submission status date: 2020-09-02 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.