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"70518-3527-0" National Drug Code (NDC)

Nebivolol 90 TABLET in 1 BOTTLE, PLASTIC (70518-3527-0)
(REMEDYREPACK INC.)

NDC Code70518-3527-0
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70518-3527-0)
Product NDC70518-3527
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20220920
Marketing Category NameANDA
Application NumberANDA203828
ManufacturerREMEDYREPACK INC.
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3527-0





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