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"72241-035-22" National Drug Code (NDC)

Nebivolol 30 TABLET in 1 BOTTLE (72241-035-22)
(Modavar Pharmaceuticals LLC)

NDC Code72241-035-22
Package Description30 TABLET in 1 BOTTLE (72241-035-22)
Product NDC72241-035
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20171229
Marketing Category NameANDA
Application NumberANDA208717
ManufacturerModavar Pharmaceuticals LLC
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72241-035-22





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