Product NDC: | 67046-020 |
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) |
Product NDC: | 67046-020 |
Labeler Name: | Contract Pharmacy Services-PA |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019787 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 19920731 |
Package NDC: | 67046-020-30 |
Package Description: | 30 TABLET in 1 BLISTER PACK (67046-020-30) |
NDC Code | 67046-020-30 |
Proprietary Name | amlodipine besylate |
Package Description | 30 TABLET in 1 BLISTER PACK (67046-020-30) |
Product NDC | 67046-020 |
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 AUTHORIZED GENERIC |
Labeler Name | Contract Pharmacy Services-PA |
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] |