"27241-182-90" National Drug Code (NDC)

Nebivolol 90 TABLET in 1 BOTTLE (27241-182-90)
(Ajanta Pharma USA Inc.)

NDC Code27241-182-90
Package Description90 TABLET in 1 BOTTLE (27241-182-90)
Product NDC27241-182
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20220331
Marketing Category NameANDA
Application NumberANDA213349
ManufacturerAjanta Pharma USA Inc.
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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