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Amlodipine Besylate - 68180-752-03 - (Amlodipine Besylate)

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Drug Information of Amlodipine Besylate

Product NDC: 68180-752
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: 68180-752
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078043
Marketing Category: ANDA
Start Marketing Date: 20070803

Package Information of Amlodipine Besylate

Package NDC: 68180-752-03
Package Description: 1000 TABLET in 1 BOTTLE (68180-752-03)

NDC Information of Amlodipine Besylate

NDC Code 68180-752-03
Proprietary Name Amlodipine Besylate
Package Description 1000 TABLET in 1 BOTTLE (68180-752-03)
Product NDC 68180-752
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine Besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070803
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, 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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