benazepril

(redirected from benazepril hydrochloride)
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be·na·ze·pril

 (bə-nā′zə-prĭl′)
n.
An ACE inhibitor drug, C24H28N2O5, used in its hydrochloride form primarily to treat hypertension and congestive heart failure.

[benz(o)- + aze(pine), seven-member ring containing nitrogen (az(o)- + (h)ep(ta)- + -ine) + -pril, ACE inhibitor suffix (from captopril).]
Translations

benazepril

n benazepril m
References in periodicals archive ?
The products are Amlodipine Besylate and Benazepril Hydrochloride capsules of 2.
Quality of Life and Extension of Survival Time, Effect of pimobendan or benazepril hydrochloride on survival times in dogs with congestive heart failure caused by naturally occurring myxomatous mitral valve disease: The QUEST study.
On January 3, 2011, Par Pharmaceutical successfully launched all strengths of amlodipine besylate and benazepril hydrochloride capsules, the generic version of Novartis' Lotrel [R] .
Adrian Boswood from the Royal Veterinary College, London, a Veterinary Cardiology Specialist and a lead-investigator on the study, explains that the independent QUEST trial set out to explore the impact on survival of Vetmedin(R) versus another current treatment, benazepril hydrochloride, an angiotensin-converting enzyme (ACE) inhibitor.
5 mm Hg, and were treated with amlodipine besylate at 5 mg, and with benazepril hydrochloride starting at 10 mg and titrated to 20 mg after 4 weeks.
Reddy's Laboratories (NYSE: RDY) announced today that it has launched Amlodipine Besylate and Benazepril Hydrochloride capsules (5 mg/40 mg and 10 mg/40 mg), a bioequivalent generic version of LOTREL([R])* capsules in the US market on July 5, 2011, following the approval by the United States Food & Drug Administration (USFDA) of Dr.
Food and Drug Administration has granted final approval for the Company's ANDA for Benazepril Hydrochloride Tablets, 5 mg, 10 mg, 20 mg and 40 mg.
NYSE: PRX) today announced that it began shipping all strengths of amlodipine besylate and benazepril hydrochloride capsules, the generic version of Novartis' Lotrel.
Food and Drug Administration (FDA) has granted final approval for Mylan Pharmaceuticals' Abbreviated New Drug Application (ANDA) for Benazepril Hydrochloride Tablets, 5 mg, 10 mg, 20 mg, and 40 mg.
s Abbreviated New Drug Application for Amlodipine Besylate and Benazepril Hydrochloride Capsules, 2.
Food and Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA) for Benazepril Hydrochloride (HCl) plus Hydrochlorothiazide (HCTZ) tablets in the same strengths as the brand, 5/6.
Available data are insufficient to show that Benazepril Hydrochloride Tablets does not have a similar risk.