Product NDC: | 54868-5761 |
Proprietary Name: | Amlodipine Besylate |
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: | 54868-5761 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078552 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070328 |
Package NDC: | 54868-5761-1 |
Package Description: | 90 TABLET in 1 BOTTLE (54868-5761-1) |
NDC Code | 54868-5761-1 |
Proprietary Name | Amlodipine Besylate |
Package Description | 90 TABLET in 1 BOTTLE (54868-5761-1) |
Product NDC | 54868-5761 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Amlodipine Besylate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20070328 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
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] |