"68462-617-30" National Drug Code (NDC)

Nebivolol 30 TABLET in 1 BOTTLE (68462-617-30)
(Glenmark Pharmaceuticals Inc., USA)

NDC Code68462-617-30
Package Description30 TABLET in 1 BOTTLE (68462-617-30)
Product NDC68462-617
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20170525
Marketing Category NameANDA
Application NumberANDA203821
ManufacturerGlenmark Pharmaceuticals Inc., USA
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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