Product NDC: | 55154-2708 |
Proprietary Name: | Norvasc |
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) |
Product NDC: | 55154-2708 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019787 |
Marketing Category: | NDA |
Start Marketing Date: | 19920731 |
Package NDC: | 55154-2708-0 |
Package Description: | 10 BLISTER PACK in 1 BAG (55154-2708-0) > 1 TABLET in 1 BLISTER PACK |
NDC Code | 55154-2708-0 |
Proprietary Name | Norvasc |
Package Description | 10 BLISTER PACK in 1 BAG (55154-2708-0) > 1 TABLET in 1 BLISTER PACK |
Product NDC | 55154-2708 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | amlodipine besylate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19920731 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
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] |