"72189-592-60" National Drug Code (NDC)

Nebivolol 60 TABLET in 1 BOTTLE (72189-592-60)
(Direct_Rx)

NDC Code72189-592-60
Package Description60 TABLET in 1 BOTTLE (72189-592-60)
Product NDC72189-592
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20241030
Marketing Category NameANDA
Application NumberANDA212682
ManufacturerDirect_Rx
Substance NameNEBIVOLOL
Strength20
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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