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"70518-3819-0" National Drug Code (NDC)
Ezetimibe 90 TABLET in 1 BOTTLE, PLASTIC (70518-3819-0)
(REMEDYREPACK INC.)
NDC Code
70518-3819-0
Package Description
90 TABLET in 1 BOTTLE, PLASTIC (70518-3819-0)
Product NDC
70518-3819
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ezetimibe
Non-Proprietary Name
Ezetimibe
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20230803
Marketing Category Name
ANDA
Application Number
ANDA211550
Manufacturer
REMEDYREPACK 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/70518-3819-0