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AMLODIPINE BESYLATE - 16729-181-58 - (Amlodipine besylate)

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Drug Information of AMLODIPINE BESYLATE

Product NDC: 16729-181
Proprietary Name: AMLODIPINE BESYLATE
Non Proprietary Name: Amlodipine besylate
Active Ingredient(s): 10    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: 16729-181
Labeler Name: Accord Healthcare Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202553
Marketing Category: ANDA
Start Marketing Date: 20130701

Package Information of AMLODIPINE BESYLATE

Package NDC: 16729-181-58
Package Description: 300 TABLET in 1 BOTTLE (16729-181-58)

NDC Information of AMLODIPINE BESYLATE

NDC Code 16729-181-58
Proprietary Name AMLODIPINE BESYLATE
Package Description 300 TABLET in 1 BOTTLE (16729-181-58)
Product NDC 16729-181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130701
Marketing Category Name ANDA
Labeler Name Accord Healthcare 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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