BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Approval overview BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE is listed in Drugs@FDA under application 078794 (ANDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Form and strength TABLET;ORAL - 20MG;25MG Sponsor APOTEX Submission history Latest submission status date: 2024-08-22 00:00:00.
Structured Monograph
Clinical summary
Approval overview BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE is listed in Drugs@FDA under application 078794 (ANDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Form and strength TABLET;ORAL - 20MG;25MG Sponsor APOTEX Submission history Latest submission status date: 2024-08-22 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.