CAPOZIDE 50/25
CAPTOPRIL; HYDROCHLOROTHIAZIDE
Approval overview CAPOZIDE 50/25 is listed in Drugs@FDA under application 018709 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient CAPTOPRIL; HYDROCHLOROTHIAZIDE Form and strength TABLET;ORAL - 50MG;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor APOTHECON Submission history Latest submission status date: 2009-02-26 00:00:00.
Structured Monograph
Clinical summary
Approval overview CAPOZIDE 50/25 is listed in Drugs@FDA under application 018709 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient CAPTOPRIL; HYDROCHLOROTHIAZIDE Form and strength TABLET;ORAL - 50MG;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor APOTHECON Submission history Latest submission status date: 2009-02-26 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.