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"67877-390-33" National Drug Code (NDC)

Nebivolol 1 BLISTER PACK in 1 CARTON (67877-390-33) / 10 TABLET in 1 BLISTER PACK
(Ascend Laboratories, LLC)

NDC Code67877-390-33
Package Description1 BLISTER PACK in 1 CARTON (67877-390-33) / 10 TABLET in 1 BLISTER PACK
Product NDC67877-390
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
Strength20
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/67877-390-33





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