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"76333-170-13" National Drug Code (NDC)
Ezetimibe 500 TABLET in 1 BOTTLE (76333-170-13)
(Orient Pharma Co., Ltd.)
NDC Code
76333-170-13
Package Description
500 TABLET in 1 BOTTLE (76333-170-13)
Product NDC
76333-170
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ezetimibe
Non-Proprietary Name
Ezetimibe
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20220630
Marketing Category Name
ANDA
Application Number
ANDA215693
Manufacturer
Orient Pharma Co., Ltd.
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/76333-170-13