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Amlodipine Besylate and Benazepril Hydrochloride - 65862-586-01 - (Amlodipine Besylate and Benazepril Hydrochloride)

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Drug Information of Amlodipine Besylate and Benazepril Hydrochloride

Product NDC: 65862-586
Proprietary Name: Amlodipine Besylate and Benazepril Hydrochloride
Non Proprietary Name: Amlodipine Besylate and Benazepril Hydrochloride
Active Ingredient(s): 10; 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: 65862-586
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202239
Marketing Category: ANDA
Start Marketing Date: 20120905

Package Information of Amlodipine Besylate and Benazepril Hydrochloride

Package NDC: 65862-586-01
Package Description: 100 CAPSULE in 1 BOTTLE (65862-586-01)

NDC Information of Amlodipine Besylate and Benazepril Hydrochloride

NDC Code 65862-586-01
Proprietary Name Amlodipine Besylate and Benazepril Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (65862-586-01)
Product NDC 65862-586
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine Besylate and Benazepril Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120905
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength Number 10; 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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