"72241-035-05" National Drug Code (NDC)

Nebivolol 100 TABLET in 1 BOTTLE (72241-035-05)
(Modavar Pharmaceuticals LLC)

NDC Code72241-035-05
Package Description100 TABLET in 1 BOTTLE (72241-035-05)
Product NDC72241-035
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20171229
Marketing Category NameANDA
Application NumberANDA208717
ManufacturerModavar Pharmaceuticals LLC
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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