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Benazepril hydrochloride; hydrochlorothiazideis the generic ingredient in two branded drugs marketed by Ani Pharms Inc, Apotex Inc, Mylan, Mylan Pharms Inc, Sandoz, Sun Pharm Inds Ltd, and Us Pharms Holdings I, and is included in eight NDAs. Additional information is available in the individual branded drug profile pages.
There are fourteen drug master file entries for benazepril hydrochloride; hydrochlorothiazide. Ten suppliers are listed for this compound.
Recent Clinical Trials for benazepril hydrochloride; hydrochlorothiazide
Identify potential brand extensions & 505(b)(2) entrants
|Shanghai Jiao Tong University School of Medicine||Phase 4|
|TSH Biopharm Corporation Limited||Phase 4|
|Ranbaxy Laboratories Limited||N/A|
Pharmacology for benazepril hydrochloride; hydrochlorothiazide
|Drug Class||Angiotensin Converting Enzyme Inhibitor |
|Mechanism of Action||Angiotensin-converting Enzyme Inhibitors |
|Physiological Effect||Decreased Blood Pressure |
|Applicant||Tradename||Generic Name||Dosage||NDA||Approval Date||Patent No.||Patent Expiration|
|Us Pharms Holdings I||LOTENSIN HCT||benazepril hydrochloride; hydrochlorothiazide||TABLET;ORAL||020033-001||May 19, 1992||Start Trial||Start Trial|
|Us Pharms Holdings I||LOTENSIN HCT||benazepril hydrochloride; hydrochlorothiazide||TABLET;ORAL||020033-003||May 19, 1992||Start Trial||Start Trial|
|Us Pharms Holdings I||LOTENSIN HCT||benazepril hydrochloride; hydrochlorothiazide||TABLET;ORAL||020033-004||May 19, 1992||Start Trial||Start Trial|
|Us Pharms Holdings I||LOTENSIN HCT||benazepril hydrochloride; hydrochlorothiazide||TABLET;ORAL||020033-002||May 19, 1992||Start Trial||Start Trial|
|>Applicant||>Tradename||>Generic Name||>Dosage||>NDA||>Approval Date||>Patent No.||>Patent Expiration|
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