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"51660-200-05" National Drug Code (NDC)
Ezetimibe 500 TABLET in 1 BOTTLE (51660-200-05)
(Ohm Laboratories Inc.)
NDC Code
51660-200-05
Package Description
500 TABLET in 1 BOTTLE (51660-200-05)
Product NDC
51660-200
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ezetimibe
Non-Proprietary Name
Ezetimibe
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20170612
Marketing Category Name
ANDA
Application Number
ANDA207311
Manufacturer
Ohm Laboratories 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/51660-200-05