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Amlodipine Besylate
Amlodipine Besylate - 0603-2109-34 - (amlodipine besylate)
Drug Information of Amlodipine Besylate
| Product NDC: | 0603-2109 |
| 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: | 0603-2109 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078414 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100407 |
Package Information of Amlodipine Besylate
| Package NDC: | 0603-2109-34 |
| Package Description: | 5000 TABLET in 1 BOTTLE, PLASTIC (0603-2109-34) |
NDC Information of Amlodipine Besylate
| NDC Code | 0603-2109-34 |
| Proprietary Name | Amlodipine Besylate |
| Package Description | 5000 TABLET in 1 BOTTLE, PLASTIC (0603-2109-34) |
| Product NDC | 0603-2109 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | amlodipine besylate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100407 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| 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] |
