"67877-392-30" National Drug Code (NDC)

Nebivolol 30 TABLET in 1 BOTTLE (67877-392-30)
(Ascend Laboratories, LLC)

NDC Code67877-392-30
Package Description30 TABLET in 1 BOTTLE (67877-392-30)
Product NDC67877-392
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
Strength5
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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