CIPRO XR
CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Approval overview CIPRO XR is listed in Drugs@FDA under application 021473 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE Form and strength TABLET, EXTENDED RELEASE;ORAL - 425.2MG;EQ 574.9MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor BAYER HLTHCARE Submission history Latest submission status date: 2021-03-30 00:00:00.
Structured Monograph
Clinical summary
Approval overview CIPRO XR is listed in Drugs@FDA under application 021473 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE Form and strength TABLET, EXTENDED RELEASE;ORAL - 425.2MG;EQ 574.9MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor BAYER HLTHCARE Submission history Latest submission status date: 2021-03-30 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.