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Amlodipine Besylate and Benazepril Hydrochloride - 0781-2271-01 - (amlodipine besylate and benazepril hydrochloride)

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Drug Information of Amlodipine Besylate and Benazepril Hydrochloride

Product NDC: 0781-2271
Proprietary Name: Amlodipine Besylate and Benazepril Hydrochloride
Non Proprietary Name: amlodipine besylate and benazepril hydrochloride
Active Ingredient(s): 2.5; 10    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: 0781-2271
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020364
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19950303

Package Information of Amlodipine Besylate and Benazepril Hydrochloride

Package NDC: 0781-2271-01
Package Description: 100 CAPSULE in 1 BOTTLE (0781-2271-01)

NDC Information of Amlodipine Besylate and Benazepril Hydrochloride

NDC Code 0781-2271-01
Proprietary Name Amlodipine Besylate and Benazepril Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (0781-2271-01)
Product NDC 0781-2271
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amlodipine besylate and benazepril hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19950303
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Sandoz Inc
Substance Name AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength Number 2.5; 10
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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