"52817-362-10" National Drug Code (NDC)

Metoprolol Tartrate 100 TABLET, FILM COATED in 1 BOTTLE (52817-362-10)
(TruPharma LLC)

NDC Code52817-362-10
Package Description100 TABLET, FILM COATED in 1 BOTTLE (52817-362-10)
Product NDC52817-362
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20181201
Marketing Category NameANDA
Application NumberANDA200981
ManufacturerTruPharma LLC
Substance NameMETOPROLOL TARTRATE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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