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"70518-3859-0" National Drug Code (NDC)

Digoxin 30 TABLET in 1 BLISTER PACK (70518-3859-0)
(REMEDYREPACK INC.)

NDC Code70518-3859-0
Package Description30 TABLET in 1 BLISTER PACK (70518-3859-0)
Product NDC70518-3859
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDigoxin
Non-Proprietary NameDigoxin
Dosage FormTABLET
UsageORAL
Start Marketing Date20230911
Marketing Category NameANDA
Application NumberANDA214982
ManufacturerREMEDYREPACK INC.
Substance NameDIGOXIN
Strength.125
Strength Unitmg/1
Pharmacy ClassesCardiac Glycoside [EPC], Cardiac Glycosides [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3859-0





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