"67877-391-01" National Drug Code (NDC)

Nebivolol 100 TABLET in 1 BOTTLE (67877-391-01)
(Ascend Laboratories, LLC)

NDC Code67877-391-01
Package Description100 TABLET in 1 BOTTLE (67877-391-01)
Product NDC67877-391
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20210916
Marketing Category NameANDA
Application NumberANDA203828
ManufacturerAscend Laboratories, LLC
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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