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Caduet
Caduet - 0069-2160-30 - (amlodipine besylate and atorvastatin calcium)
Drug Information of Caduet
| Product NDC: | 0069-2160 |
| Proprietary Name: | Caduet |
| Non Proprietary Name: | amlodipine besylate and atorvastatin calcium |
| Active Ingredient(s): | 10; 10 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 Caduet
| Product NDC: | 0069-2160 |
| Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021540 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040130 |
Package Information of Caduet
| Package NDC: | 0069-2160-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (0069-2160-30) |
NDC Information of Caduet
| NDC Code | 0069-2160-30 |
| Proprietary Name | Caduet |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0069-2160-30) |
| Product NDC | 0069-2160 |
| 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 | 20040130 |
| Marketing Category Name | NDA |
| Labeler Name | Pfizer Laboratories Div Pfizer Inc |
| Substance Name | AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM |
| Strength Number | 10; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
