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Amlodipine besylate - 0143-9959-01 - (Amlodipine besylate)

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Drug Information of Amlodipine besylate

Product NDC: 0143-9959
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: 0143-9959
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077771
Marketing Category: ANDA
Start Marketing Date: 20110412

Package Information of Amlodipine besylate

Package NDC: 0143-9959-01
Package Description: 100 TABLET in 1 BOTTLE (0143-9959-01)

NDC Information of Amlodipine besylate

NDC Code 0143-9959-01
Proprietary Name Amlodipine besylate
Package Description 100 TABLET in 1 BOTTLE (0143-9959-01)
Product NDC 0143-9959
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110412
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
Substance Name AMLODIPINE
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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