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Amlodipine besylate - 76282-238-10 - (Amlodipine besylate)

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Drug Information of Amlodipine besylate

Product NDC: 76282-238
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: 76282-238
Labeler Name: Exelan Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077955
Marketing Category: ANDA
Start Marketing Date: 20071102

Package Information of Amlodipine besylate

Package NDC: 76282-238-10
Package Description: 1000 TABLET in 1 BOTTLE (76282-238-10)

NDC Information of Amlodipine besylate

NDC Code 76282-238-10
Proprietary Name Amlodipine besylate
Package Description 1000 TABLET in 1 BOTTLE (76282-238-10)
Product NDC 76282-238
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071102
Marketing Category Name ANDA
Labeler Name Exelan Pharmaceuticals, 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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