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Amlodipine besylate/atorvastatin calcium
Amlodipine besylate/atorvastatin calcium - 0378-6162-05 - (AMLODIPINE BESYLATE and ATORVASTATIN CALCIUM)
Drug Information of Amlodipine besylate/atorvastatin calcium
| Product NDC: | 0378-6162 |
| Proprietary Name: | Amlodipine besylate/atorvastatin calcium |
| Non Proprietary Name: | AMLODIPINE BESYLATE and ATORVASTATIN CALCIUM |
| Active Ingredient(s): | 2.5; 20 mg/1; mg/1 & nbsp; AMLODIPINE BESYLATE and ATORVASTATIN CALCIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amlodipine besylate/atorvastatin calcium
| Product NDC: | 0378-6162 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021540 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20111130 |
Package Information of Amlodipine besylate/atorvastatin calcium
| Package NDC: | 0378-6162-05 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE (0378-6162-05) |
NDC Information of Amlodipine besylate/atorvastatin calcium
| NDC Code | 0378-6162-05 |
| Proprietary Name | Amlodipine besylate/atorvastatin calcium |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (0378-6162-05) |
| Product NDC | 0378-6162 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AMLODIPINE BESYLATE and ATORVASTATIN CALCIUM |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111130 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM |
| Strength Number | 2.5; 20 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
