"70518-1250-0" National Drug Code (NDC)

Digoxin 30 TABLET in 1 BLISTER PACK (70518-1250-0)
(REMEDYREPACK INC.)

NDC Code70518-1250-0
Package Description30 TABLET in 1 BLISTER PACK (70518-1250-0)
Product NDC70518-1250
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDigoxin
Non-Proprietary NameDigoxin
Dosage FormTABLET
UsageORAL
Start Marketing Date20180611
Marketing Category NameANDA
Application NumberANDA077002
ManufacturerREMEDYREPACK INC.
Substance NameDIGOXIN
Strength125
Strength Unitug/1
Pharmacy ClassesCardiac Glycoside [EPC],Cardiac Glycosides [CS]

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