FLEXERIL
CYCLOBENZAPRINE HYDROCHLORIDE
Approval overview FLEXERIL is listed in Drugs@FDA under application 017821 (NDA).
Review priority: UNKNOWN Marketing status: Discontinued Active ingredient CYCLOBENZAPRINE HYDROCHLORIDE Form and strength TABLET;ORAL - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor JANSSEN RES AND DEV Submission history Latest submission status date: 2013-04-11 00:00:00.
Structured Monograph
Clinical summary
Approval overview FLEXERIL is listed in Drugs@FDA under application 017821 (NDA). Review priority: UNKNOWN Marketing status: Discontinued Active ingredient CYCLOBENZAPRINE HYDROCHLORIDE Form and strength TABLET;ORAL - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor JANSSEN RES AND DEV Submission history Latest submission status date: 2013-04-11 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: UNKNOWN
Interaction Notes
- No interaction notes stored yet.