"59762-0812-1" National Drug Code (NDC)

Nadolol 100 TABLET in 1 BOTTLE (59762-0812-1)
(Greenstone LLC)

NDC Code59762-0812-1
Package Description100 TABLET in 1 BOTTLE (59762-0812-1)
Product NDC59762-0812
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNadolol
Non-Proprietary NameNadolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20140428
End Marketing Date20230831
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA018063
ManufacturerGreenstone LLC
Substance NameNADOLOL
Strength80
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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