"61786-761-19" National Drug Code (NDC)

Metoprolol Tartrate 90 TABLET, FILM COATED in 1 BOTTLE (61786-761-19)
(REMEDYREPACK INC.)

NDC Code61786-761-19
Package Description90 TABLET, FILM COATED in 1 BOTTLE (61786-761-19)
Product NDC61786-761
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160628
Marketing Category NameANDA
Application NumberANDA077739
ManufacturerREMEDYREPACK INC.
Substance NameMETOPROLOL TARTRATE
Strength50
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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