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VYTORIN
VYTORIN - 66582-313-27 - (ezetimibe and simvastatin)
Drug Information of VYTORIN
| Product NDC: | 66582-313 |
| Proprietary Name: | VYTORIN |
| Non Proprietary Name: | ezetimibe and simvastatin |
| Active Ingredient(s): | 10; 40 mg/1; mg/1 & nbsp; ezetimibe and simvastatin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VYTORIN
| Product NDC: | 66582-313 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021687 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040723 |
Package Information of VYTORIN
| Package NDC: | 66582-313-27 |
| Package Description: | 4 BLISTER PACK in 1 CARTON (66582-313-27) > 7 TABLET in 1 BLISTER PACK |
NDC Information of VYTORIN
| NDC Code | 66582-313-27 |
| Proprietary Name | VYTORIN |
| Package Description | 4 BLISTER PACK in 1 CARTON (66582-313-27) > 7 TABLET in 1 BLISTER PACK |
| Product NDC | 66582-313 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ezetimibe and simvastatin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040723 |
| Marketing Category Name | NDA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | EZETIMIBE; SIMVASTATIN |
| Strength Number | 10; 40 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Decreased Cholesterol Absorption [PE],Dietary Cholesterol Absorption Inhibitor [EPC],HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
