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Amlodipine
Amlodipine - 33342-015-12 - (Amlodipine)
Drug Information of Amlodipine
| Product NDC: | 33342-015 |
| Proprietary Name: | Amlodipine |
| Non Proprietary Name: | Amlodipine |
| Active Ingredient(s): | 5 mg/1 & nbsp; Amlodipine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amlodipine
| Product NDC: | 33342-015 |
| Labeler Name: | Macleods Pharmaceuticals Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201380 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120413 |
Package Information of Amlodipine
| Package NDC: | 33342-015-12 |
| Package Description: | 100 TABLET in 1 CARTON (33342-015-12) |
NDC Information of Amlodipine
| NDC Code | 33342-015-12 |
| Proprietary Name | Amlodipine |
| Package Description | 100 TABLET in 1 CARTON (33342-015-12) |
| Product NDC | 33342-015 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amlodipine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120413 |
| Marketing Category Name | ANDA |
| Labeler Name | Macleods Pharmaceuticals Limited |
| 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] |
