EXELON
RIVASTIGMINE TARTRATE
Approval overview EXELON is listed in Drugs@FDA under application 020823 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient RIVASTIGMINE TARTRATE Form and strength CAPSULE;ORAL - EQ 6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor NOVARTIS Submission history Latest submission status date: 2018-12-18 00:00:00.
Structured Monograph
Clinical summary
Approval overview EXELON is listed in Drugs@FDA under application 020823 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient RIVASTIGMINE TARTRATE Form and strength CAPSULE;ORAL - EQ 6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor NOVARTIS Submission history Latest submission status date: 2018-12-18 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.