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Amlodipine Besylate and Benazepril Hydrochloride - 0378-6900-01 - (amlodipine besylate and benazepril hydrochloride)

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Drug Information of Amlodipine Besylate and Benazepril Hydrochloride

Product NDC: 0378-6900
Proprietary Name: Amlodipine Besylate and Benazepril Hydrochloride
Non Proprietary Name: amlodipine besylate and benazepril hydrochloride
Active Ingredient(s): 10; 40    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: 0378-6900
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079047
Marketing Category: ANDA
Start Marketing Date: 20130510

Package Information of Amlodipine Besylate and Benazepril Hydrochloride

Package NDC: 0378-6900-01
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-6900-01)

NDC Information of Amlodipine Besylate and Benazepril Hydrochloride

NDC Code 0378-6900-01
Proprietary Name Amlodipine Besylate and Benazepril Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-6900-01)
Product NDC 0378-6900
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amlodipine besylate and benazepril hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130510
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength Number 10; 40
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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