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Amlodipine Besylate - 54458-903-02 - (Amlodipine)

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Drug Information of Amlodipine Besylate

Product NDC: 54458-903
Proprietary Name: Amlodipine Besylate
Non Proprietary Name: Amlodipine
Active Ingredient(s): 10    mg/1 & nbsp;   Amlodipine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Amlodipine Besylate

Product NDC: 54458-903
Labeler Name: International Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078925
Marketing Category: ANDA
Start Marketing Date: 20120914

Package Information of Amlodipine Besylate

Package NDC: 54458-903-02
Package Description: 30 TABLET in 1 BLISTER PACK (54458-903-02)

NDC Information of Amlodipine Besylate

NDC Code 54458-903-02
Proprietary Name Amlodipine Besylate
Package Description 30 TABLET in 1 BLISTER PACK (54458-903-02)
Product NDC 54458-903
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120914
Marketing Category Name ANDA
Labeler Name International Labs, Inc.
Substance Name AMLODIPINE BESYLATE
Strength Number 10
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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