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"51660-200-90" National Drug Code (NDC)

Ezetimibe 90 TABLET in 1 BOTTLE (51660-200-90)
(Ohm Laboratories Inc.)

NDC Code51660-200-90
Package Description90 TABLET in 1 BOTTLE (51660-200-90)
Product NDC51660-200
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEzetimibe
Non-Proprietary NameEzetimibe
Dosage FormTABLET
UsageORAL
Start Marketing Date20170612
Marketing Category NameANDA
Application NumberANDA207311
ManufacturerOhm Laboratories Inc.
Substance NameEZETIMIBE
Strength10
Strength Unitmg/1
Pharmacy ClassesDecreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51660-200-90





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