"68001-220-00" National Drug Code (NDC)

Nadolol 100 TABLET in 1 BOTTLE (68001-220-00)
(BluePoint Laboratories)

NDC Code68001-220-00
Package Description100 TABLET in 1 BOTTLE (68001-220-00)
Product NDC68001-220
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNadolol
Non-Proprietary NameNadolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20140205
Marketing Category NameANDA
Application NumberANDA074501
ManufacturerBluePoint Laboratories
Substance NameNADOLOL
Strength40
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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