"68001-319-00" National Drug Code (NDC)

Nadolol 100 TABLET in 1 BOTTLE (68001-319-00)
(BluePoint Laboratories)

NDC Code68001-319-00
Package Description100 TABLET in 1 BOTTLE (68001-319-00)
Product NDC68001-319
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNadolol
Non-Proprietary NameNadolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20160223
Marketing Category NameANDA
Application NumberANDA203455
ManufacturerBluePoint Laboratories
Substance NameNADOLOL
Strength80
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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