"70756-025-30" National Drug Code (NDC)

Nebivolol 30 TABLET in 1 BOTTLE (70756-025-30)
(Lifestar Pharma LLC)

NDC Code70756-025-30
Package Description30 TABLET in 1 BOTTLE (70756-025-30)
Product NDC70756-025
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20221114
Marketing Category NameANDA
Application NumberANDA216172
ManufacturerLifestar Pharma LLC
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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