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Amlodipine Besylate - 0093-7168-98 - (Amlodipine Besylate)

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Drug Information of Amlodipine Besylate

Product NDC: 0093-7168
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: 0093-7168
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076846
Marketing Category: ANDA
Start Marketing Date: 20070710

Package Information of Amlodipine Besylate

Package NDC: 0093-7168-98
Package Description: 90 TABLET in 1 BOTTLE (0093-7168-98)

NDC Information of Amlodipine Besylate

NDC Code 0093-7168-98
Proprietary Name Amlodipine Besylate
Package Description 90 TABLET in 1 BOTTLE (0093-7168-98)
Product NDC 0093-7168
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine Besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070710
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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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