"0904-7189-04" National Drug Code (NDC)

Nebivolol 30 BLISTER PACK in 1 CARTON (0904-7189-04) / 1 TABLET in 1 BLISTER PACK
(Major Pharmaceuticals)

NDC Code0904-7189-04
Package Description30 BLISTER PACK in 1 CARTON (0904-7189-04) / 1 TABLET in 1 BLISTER PACK
Product NDC0904-7189
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20180302
End Marketing Date20250430
Marketing Category NameANDA
Application NumberANDA203966
ManufacturerMajor Pharmaceuticals
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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