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Amlodipine Besylate and Benazepril Hydrochloride - 43063-233-60 - (amlodipine besylate and benazepril hydrochloride)

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Drug Information of Amlodipine Besylate and Benazepril Hydrochloride

Product NDC: 43063-233
Proprietary Name: Amlodipine Besylate and Benazepril Hydrochloride
Non Proprietary Name: amlodipine besylate and benazepril hydrochloride
Active Ingredient(s): 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: 43063-233
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020364
Marketing Category: NDA
Start Marketing Date: 19950303

Package Information of Amlodipine Besylate and Benazepril Hydrochloride

Package NDC: 43063-233-60
Package Description: 60 CAPSULE in 1 BOTTLE, PLASTIC (43063-233-60)

NDC Information of Amlodipine Besylate and Benazepril Hydrochloride

NDC Code 43063-233-60
Proprietary Name Amlodipine Besylate and Benazepril Hydrochloride
Package Description 60 CAPSULE in 1 BOTTLE, PLASTIC (43063-233-60)
Product NDC 43063-233
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
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength Number 5; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiotensin 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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