"0781-1507-10" National Drug Code (NDC)

Atenolol 1000 TABLET in 1 BOTTLE (0781-1507-10)
(Sandoz Inc)

NDC Code0781-1507-10
Package Description1000 TABLET in 1 BOTTLE (0781-1507-10)
Product NDC0781-1507
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAtenolol
Non-Proprietary NameAtenolol
Dosage FormTABLET
UsageORAL
Start Marketing Date19910917
End Marketing Date20211231
Marketing Category NameANDA
Application NumberANDA073026
ManufacturerSandoz Inc
Substance NameATENOLOL
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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