"82009-024-05" National Drug Code (NDC)

Ezetimibe 500 TABLET in 1 BOTTLE (82009-024-05)
(Quallent Pharmaceuticals Health LLC)

NDC Code82009-024-05
Package Description500 TABLET in 1 BOTTLE (82009-024-05)
Product NDC82009-024
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEzetimibe
Non-Proprietary NameEzetimibe
Dosage FormTABLET
UsageORAL
Start Marketing Date20220820
Marketing Category NameANDA
Application NumberANDA204331
ManufacturerQuallent Pharmaceuticals Health LLC
Substance NameEZETIMIBE
Strength10
Strength Unitmg/1
Pharmacy ClassesDecreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC]

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