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Amlodipine Besylate - 0054-0101-28 - (Amlodipine Besylate)

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Drug Information of Amlodipine Besylate

Product NDC: 0054-0101
Proprietary Name: Amlodipine Besylate
Non Proprietary Name: Amlodipine Besylate
Active Ingredient(s): 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: 0054-0101
Labeler Name: Roxane Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077262
Marketing Category: ANDA
Start Marketing Date: 20070709

Package Information of Amlodipine Besylate

Package NDC: 0054-0101-28
Package Description: 300 TABLET in 1 BOTTLE (0054-0101-28)

NDC Information of Amlodipine Besylate

NDC Code 0054-0101-28
Proprietary Name Amlodipine Besylate
Package Description 300 TABLET in 1 BOTTLE (0054-0101-28)
Product NDC 0054-0101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine Besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070709
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, Inc
Substance Name AMLODIPINE BESYLATE
Strength Number 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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