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Amlodipine Besylate and Benazepril Hydrochloride - 54868-5793-1 - (Amlodipine Besylate and Benazepril Hydrochloride)

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Drug Information of Amlodipine Besylate and Benazepril Hydrochloride

Product NDC: 54868-5793
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: 54868-5793
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078466
Marketing Category: ANDA
Start Marketing Date: 20100816

Package Information of Amlodipine Besylate and Benazepril Hydrochloride

Package NDC: 54868-5793-1
Package Description: 30 CAPSULE in 1 BOTTLE (54868-5793-1)

NDC Information of Amlodipine Besylate and Benazepril Hydrochloride

NDC Code 54868-5793-1
Proprietary Name Amlodipine Besylate and Benazepril Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE (54868-5793-1)
Product NDC 54868-5793
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine Besylate and Benazepril Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100816
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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