COMBIPRES
CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE
Approval overview COMBIPRES is listed in Drugs@FDA under application 017503 (NDA).
Review priority: PRIORITY Marketing status: Discontinued Active ingredient CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE Form and strength TABLET;ORAL - 15MG;0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor BOEHRINGER INGELHEIM Submission history Latest submission status date: 1999-09-15 00:00:00.
Structured Monograph
Clinical summary
Approval overview COMBIPRES is listed in Drugs@FDA under application 017503 (NDA). Review priority: PRIORITY Marketing status: Discontinued Active ingredient CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE Form and strength TABLET;ORAL - 15MG;0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor BOEHRINGER INGELHEIM Submission history Latest submission status date: 1999-09-15 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: PRIORITY
Interaction Notes
- No interaction notes stored yet.