Details for New Drug Application (NDA): 211663
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The generic ingredient in EZETIMIBE AND SIMVASTATIN is ezetimibe; simvastatin. There are twenty-four drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the ezetimibe; simvastatin profile page.
Summary for 211663
| Tradename: | EZETIMIBE AND SIMVASTATIN |
| Applicant: | Sciegen Pharms |
| Ingredient: | ezetimibe; simvastatin |
| Patents: | 0 |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 10MG;10MG | ||||
| Approval Date: | Dec 10, 2024 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 10MG;20MG | ||||
| Approval Date: | Dec 10, 2024 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 10MG;40MG | ||||
| Approval Date: | Dec 10, 2024 | TE: | RLD: | No | |||||
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