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Zetia
Zetia - 21695-778-90 - (Ezetimibe)
Drug Information of Zetia
| Product NDC: | 21695-778 |
| Proprietary Name: | Zetia |
| Non Proprietary Name: | Ezetimibe |
| Active Ingredient(s): | 10 mg/1 & nbsp; Ezetimibe |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zetia
| Product NDC: | 21695-778 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021445 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090727 |
Package Information of Zetia
| Package NDC: | 21695-778-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (21695-778-90) |
NDC Information of Zetia
| NDC Code | 21695-778-90 |
| Proprietary Name | Zetia |
| Package Description | 90 TABLET in 1 BOTTLE (21695-778-90) |
| Product NDC | 21695-778 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ezetimibe |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090727 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | EZETIMIBE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Cholesterol Absorption [PE],Dietary Cholesterol Absorption Inhibitor [EPC] |
