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AMLODIPINE BESYLATE - 55648-422-04 - (AMLODIPINE BESYLATE)

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Drug Information of AMLODIPINE BESYLATE

Product NDC: 55648-422
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: 55648-422
Labeler Name: WOCKHARDT LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078500
Marketing Category: ANDA
Start Marketing Date: 20070906

Package Information of AMLODIPINE BESYLATE

Package NDC: 55648-422-04
Package Description: 100 TABLET in 1 BOTTLE (55648-422-04)

NDC Information of AMLODIPINE BESYLATE

NDC Code 55648-422-04
Proprietary Name AMLODIPINE BESYLATE
Package Description 100 TABLET in 1 BOTTLE (55648-422-04)
Product NDC 55648-422
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMLODIPINE BESYLATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070906
Marketing Category Name ANDA
Labeler Name WOCKHARDT LIMITED
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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