"71335-2516-1" National Drug Code (NDC)

Nebivolol 30 TABLET in 1 BOTTLE (71335-2516-1)
(Bryant Ranch Prepack)

NDC Code71335-2516-1
Package Description30 TABLET in 1 BOTTLE (71335-2516-1)
Product NDC71335-2516
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20220214
Marketing Category NameANDA
Application NumberANDA212682
ManufacturerBryant Ranch Prepack
Substance NameNEBIVOLOL
Strength5
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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