| Product NDC: | 68645-445 |
| 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: | 68645-445 |
| Labeler Name: | Legacy Pharmaceutical Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077995 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110101 |
| Package NDC: | 68645-445-70 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (68645-445-70) |
| NDC Code | 68645-445-70 |
| Proprietary Name | Amlodipine Besylate |
| Package Description | 30 TABLET in 1 BLISTER PACK (68645-445-70) |
| Product NDC | 68645-445 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amlodipine Besylate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110101 |
| Marketing Category Name | ANDA |
| Labeler Name | Legacy Pharmaceutical Packaging |
| 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] |