"71335-2648-2" National Drug Code (NDC)

Nebivolol 90 TABLET in 1 BOTTLE (71335-2648-2)
(Bryant Ranch Prepack)

NDC Code71335-2648-2
Package Description90 TABLET in 1 BOTTLE (71335-2648-2)
Product NDC71335-2648
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20241001
Marketing Category NameANDA
Application NumberANDA217397
ManufacturerBryant Ranch Prepack
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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