"43975-251-10" National Drug Code (NDC)

Nebivolol 100 TABLET in 1 BOTTLE (43975-251-10)
(Amerigen Pharmaceuticals Inc.)

NDC Code43975-251-10
Package Description100 TABLET in 1 BOTTLE (43975-251-10)
Product NDC43975-251
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20150428
Marketing Category NameANDA
Application NumberANDA203659
ManufacturerAmerigen Pharmaceuticals Inc.
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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