"70518-1979-2" National Drug Code (NDC)

Metoprolol Tartrate 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1979-2)
(REMEDYREPACK INC.)

NDC Code70518-1979-2
Package Description180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1979-2)
Product NDC70518-1979
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190326
Marketing Category NameANDA
Application NumberANDA077739
ManufacturerREMEDYREPACK INC.
Substance NameMETOPROLOL TARTRATE
Strength25
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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