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"50228-379-10" National Drug Code (NDC)
Ezetimibe 1000 TABLET in 1 BOTTLE (50228-379-10)
(ScieGen Pharmaceuticals Inc)
NDC Code
50228-379-10
Package Description
1000 TABLET in 1 BOTTLE (50228-379-10)
Product NDC
50228-379
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ezetimibe
Non-Proprietary Name
Ezetimibe
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20201023
Marketing Category Name
ANDA
Application Number
ANDA210673
Manufacturer
ScieGen Pharmaceuticals Inc
Substance Name
EZETIMIBE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Decreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50228-379-10