"70518-2139-0" National Drug Code (NDC)

Nadolol 90 TABLET in 1 BOTTLE, PLASTIC (70518-2139-0)
(REMEDYREPACK INC.)

NDC Code70518-2139-0
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70518-2139-0)
Product NDC70518-2139
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNadolol
Non-Proprietary NameNadolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20190610
Marketing Category NameANDA
Application NumberANDA207761
ManufacturerREMEDYREPACK INC.
Substance NameNADOLOL
Strength40
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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