"70518-1354-1" National Drug Code (NDC)

Metoprolol Tartrate 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1354-1)
(REMEDYREPACK INC.)

NDC Code70518-1354-1
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1354-1)
Product NDC70518-1354
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180808
Marketing Category NameANDA
Application NumberANDA076704
ManufacturerREMEDYREPACK INC.
Substance NameMETOPROLOL TARTRATE
Strength25
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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