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amlodipine besylate
amlodipine besylate - 59762-1530-5 - (AMLODIPINE BESYLATE)
Drug Information of amlodipine besylate
| Product NDC: | 59762-1530 |
| 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: | 59762-1530 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019787 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20070323 |
Package Information of amlodipine besylate
| Package NDC: | 59762-1530-5 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (59762-1530-5) > 1 TABLET in 1 BLISTER PACK (59762-1530-6) |
NDC Information of amlodipine besylate
| NDC Code | 59762-1530-5 |
| Proprietary Name | amlodipine besylate |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (59762-1530-5) > 1 TABLET in 1 BLISTER PACK (59762-1530-6) |
| Product NDC | 59762-1530 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AMLODIPINE BESYLATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070323 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| 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] |
