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Amlodipine Besylate - 50436-7076-1 - (amlodipine besylate)

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Drug Information of Amlodipine Besylate

Product NDC: 50436-7076
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: 50436-7076
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078414
Marketing Category: ANDA
Start Marketing Date: 20100407

Package Information of Amlodipine Besylate

Package NDC: 50436-7076-1
Package Description: 30 TABLET in 1 BOTTLE (50436-7076-1)

NDC Information of Amlodipine Besylate

NDC Code 50436-7076-1
Proprietary Name Amlodipine Besylate
Package Description 30 TABLET in 1 BOTTLE (50436-7076-1)
Product NDC 50436-7076
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amlodipine besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100407
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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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