"72603-872-01" National Drug Code (NDC)

Nebivolol 30 TABLET in 1 BOTTLE (72603-872-01)
(NorthStar RxLLC)

NDC Code72603-872-01
Package Description30 TABLET in 1 BOTTLE (72603-872-01)
Product NDC72603-872
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20250714
Marketing Category NameANDA
Application NumberANDA212661
ManufacturerNorthStar RxLLC
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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