Product NDC: | 49999-478 |
Proprietary Name: | Norvasc |
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) |
Product NDC: | 49999-478 |
Labeler Name: | Lake Erie Medical & Surgical Supplies DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019787 |
Marketing Category: | NDA |
Start Marketing Date: | 20111122 |
Package NDC: | 49999-478-90 |
Package Description: | 90 TABLET in 1 BOTTLE (49999-478-90) |
NDC Code | 49999-478-90 |
Proprietary Name | Norvasc |
Package Description | 90 TABLET in 1 BOTTLE (49999-478-90) |
Product NDC | 49999-478 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | amlodipine besylate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20111122 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical & Surgical Supplies DBA Quality Care Products LLC |
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] |