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| Product NDC Code | 70771-1109 | ||||||||||||||
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| Drug Name | Ezetimibe |
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| Type | Generic | ||||||||||||||
| Pharm Class | Decreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC] |
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| Active Ingredients |
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| Route | ORAL | ||||||||||||||
| Dosage Form | TABLET | ||||||||||||||
| RxCUI drug identifier | 349556 | ||||||||||||||
| Application Number | ANDA204331 | ||||||||||||||
| Labeler Name | Zydus Lifesciences Limited | ||||||||||||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Spl product data elements
Usually a list of ingredients in a drug product.ezetimibe ezetimibe EZETIMIBE EZETIMIBE CELLULOSE, MICROCRYSTALLINE CROSPOVIDONE LACTOSE MONOHYDRATE MAGNESIUM STEARATE POVIDONE SODIUM LAURYL SULFATE SODIUM STEARYL FUMARATE STARCH, CORN WHITE TO OFF-WHITE CAPSULE 773
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.NDC 70771-1109-3 in bottle of 30 tablets Ezetimibe Tablets , 10 mg Rx only 30 tablets Ezetimibe Tablets, 10 mg
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API