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amlodipine besylate - 59762-1530-2 - (AMLODIPINE BESYLATE)

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Drug Information of amlodipine besylate

Product NDC: 59762-1530
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: 59762-1530
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019787
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20070323

Package Information of amlodipine besylate

Package NDC: 59762-1530-2
Package Description: 300 TABLET in 1 BOTTLE (59762-1530-2)

NDC Information of amlodipine besylate

NDC Code 59762-1530-2
Proprietary Name amlodipine besylate
Package Description 300 TABLET in 1 BOTTLE (59762-1530-2)
Product NDC 59762-1530
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMLODIPINE BESYLATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070323
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
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


General Information