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Amlodipine Besylate - 65862-101-99 - (Amlodipine Besylate)

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Drug Information of Amlodipine Besylate

Product NDC: 65862-101
Proprietary Name: Amlodipine Besylate
Non Proprietary Name: Amlodipine Besylate
Active Ingredient(s): 2.5    mg/1 & nbsp;   Amlodipine Besylate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Amlodipine Besylate

Product NDC: 65862-101
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078021
Marketing Category: ANDA
Start Marketing Date: 20070717

Package Information of Amlodipine Besylate

Package NDC: 65862-101-99
Package Description: 1000 TABLET in 1 BOTTLE (65862-101-99)

NDC Information of Amlodipine Besylate

NDC Code 65862-101-99
Proprietary Name Amlodipine Besylate
Package Description 1000 TABLET in 1 BOTTLE (65862-101-99)
Product NDC 65862-101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine Besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070717
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name AMLODIPINE BESYLATE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Amlodipine Besylate


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