"70518-4032-0" National Drug Code (NDC)

Nebivolol 90 TABLET in 1 BOTTLE, PLASTIC (70518-4032-0)
(REMEDYREPACK INC.)

NDC Code70518-4032-0
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70518-4032-0)
Product NDC70518-4032
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20240305
Marketing Category NameANDA
Application NumberANDA212682
ManufacturerREMEDYREPACK INC.
Substance NameNEBIVOLOL
Strength5
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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