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Amlodipine Besylate and Benazepril Hydrochloride - 0093-7372-10 - (Amlodipine Besylate and Benazepril Hydrochloride)

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Drug Information of Amlodipine Besylate and Benazepril Hydrochloride

Product NDC: 0093-7372
Proprietary Name: Amlodipine Besylate and Benazepril Hydrochloride
Non Proprietary Name: Amlodipine Besylate and Benazepril Hydrochloride
Active Ingredient(s): 5; 20    mg/1; mg/1 & nbsp;   Amlodipine Besylate and Benazepril Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Amlodipine Besylate and Benazepril Hydrochloride

Product NDC: 0093-7372
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077179
Marketing Category: ANDA
Start Marketing Date: 20070521

Package Information of Amlodipine Besylate and Benazepril Hydrochloride

Package NDC: 0093-7372-10
Package Description: 1000 CAPSULE in 1 BOTTLE (0093-7372-10)

NDC Information of Amlodipine Besylate and Benazepril Hydrochloride

NDC Code 0093-7372-10
Proprietary Name Amlodipine Besylate and Benazepril Hydrochloride
Package Description 1000 CAPSULE in 1 BOTTLE (0093-7372-10)
Product NDC 0093-7372
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine Besylate and Benazepril Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070521
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength Number 5; 20
Strength Unit mg/1; mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

Complete Information of Amlodipine Besylate and Benazepril Hydrochloride


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