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amlodipine besylate
amlodipine besylate - 0832-0043-01 - (amlodipine besylate)
Drug Information of amlodipine besylate
| Product NDC: | 0832-0043 |
| 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) |
Labeler Information of amlodipine besylate
| Product NDC: | 0832-0043 |
| Labeler Name: | Upsher-Smith Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077759 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070709 |
Package Information of amlodipine besylate
| Package NDC: | 0832-0043-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (0832-0043-01) > 10 TABLET in 1 BLISTER PACK (0832-0043-89) |
NDC Information of amlodipine besylate
| NDC Code | 0832-0043-01 |
| Proprietary Name | amlodipine besylate |
| Package Description | 10 BLISTER PACK in 1 CARTON (0832-0043-01) > 10 TABLET in 1 BLISTER PACK (0832-0043-89) |
| Product NDC | 0832-0043 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | amlodipine besylate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070709 |
| Marketing Category Name | ANDA |
| Labeler Name | Upsher-Smith Laboratories, 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] |
