MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE
Approval overview MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE is listed in Drugs@FDA under application 202150 (ANDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE Form and strength TABLET;ORAL - 12.5MG;15MG Sponsor HERITAGE Submission history Latest submission status date: 2020-08-20 00:00:00.
Structured Monograph
Clinical summary
Approval overview MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE is listed in Drugs@FDA under application 202150 (ANDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE Form and strength TABLET;ORAL - 12.5MG;15MG Sponsor HERITAGE Submission history Latest submission status date: 2020-08-20 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.