"71209-059-01" National Drug Code (NDC)

Nebivolol 30 TABLET in 1 BOTTLE (71209-059-01)
(Cadila Pharmaceuticals Limited)

NDC Code71209-059-01
Package Description30 TABLET in 1 BOTTLE (71209-059-01)
Product NDC71209-059
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20171229
Marketing Category NameANDA
Application NumberANDA208717
ManufacturerCadila Pharmaceuticals Limited
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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