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amlodipine besylate - 0832-0043-09 - (amlodipine besylate)

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Drug Information of amlodipine besylate

Product NDC: 0832-0043
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: 0832-0043
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077759
Marketing Category: ANDA
Start Marketing Date: 20070709

Package Information of amlodipine besylate

Package NDC: 0832-0043-09
Package Description: 90 TABLET in 1 BOTTLE (0832-0043-09)

NDC Information of amlodipine besylate

NDC Code 0832-0043-09
Proprietary Name amlodipine besylate
Package Description 90 TABLET in 1 BOTTLE (0832-0043-09)
Product NDC 0832-0043
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 Upsher-Smith 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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