"62559-278-05" National Drug Code (NDC)

Nebivolol 500 TABLET in 1 BOTTLE (62559-278-05)
(ANI Pharmaceuticals, Inc.)

NDC Code62559-278-05
Package Description500 TABLET in 1 BOTTLE (62559-278-05)
Product NDC62559-278
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20210917
Marketing Category NameANDA
Application NumberANDA203659
ManufacturerANI Pharmaceuticals, Inc.
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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