General MedicationsINTRAVENOUSStandard
CYTALUX
PAFOLACIANINE SODIUM
Standard Dose
EQ 3.2MG BASE/1.6ML (EQ 2MG BASE/ML)
Max Dose
Refer to approved labeling
Primary Use
Review priority: PRIORITY Marketing status: Prescription
Summary
Approval overview CYTALUX is listed in Drugs@FDA under application 214907 (NDA).
Review priority: PRIORITY Marketing status: Prescription Active ingredient PAFOLACIANINE SODIUM Form and strength SOLUTION;INTRAVENOUS - EQ 3.2MG BASE/1.6ML (EQ 2MG BASE/ML) Sponsor ON TARGET LABS Submission history Latest submission status date: 2022-12-16 00:00:00.
Structured Monograph
Clinical summary
Approval overview CYTALUX is listed in Drugs@FDA under application 214907 (NDA). Review priority: PRIORITY Marketing status: Prescription Active ingredient PAFOLACIANINE SODIUM Form and strength SOLUTION;INTRAVENOUS - EQ 3.2MG BASE/1.6ML (EQ 2MG BASE/ML) Sponsor ON TARGET LABS Submission history Latest submission status date: 2022-12-16 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Prescription
- • Review priority: PRIORITY
Interaction Notes
- No interaction notes stored yet.