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 ?
com been reported for the determination of benazepril hydrochloride alone by HPLC [37-39], HPTLC [40], CE [41-43] GC-MS [44-45], LC-MS [46-47], spectrophotometric detection [48-49] and by voltammetry [50] from pharmaceutical dosages form.
The products are Amlodipine Besylate and Benazepril Hydrochloride capsules of 2.
Reddya[euro](tm)s Laboratories unveils Amlodipine Besylate and Benazepril Hydrochloride capsules, 5 mg/40 mg and 10 mg/40 mg(C)2011 M2 COMMUNICATIONS http://www.
On January 3, 2011, Par Pharmaceutical successfully launched all strengths of amlodipine besylate and benazepril hydrochloride capsules, the generic version of Novartis' Lotrel [R] .
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.
Specialty pharmaceutical company Par Pharmaceutical Companies Inc (NYSE:PRX) said on Monday that it has commenced the shipment of all strengths (5/320mg and 10/320mg strengths) of amlodipine besylate and benazepril hydrochloride capsules, which are indicated for the treatment of hypertension in patients not adequately controlled on monotherapy with either agent.
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.
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.
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.