"61919-726-90" National Drug Code (NDC)

Metoprolol Tartrate 90 TABLET, FILM COATED in 1 BOTTLE (61919-726-90)
(DIRECT RX)

NDC Code61919-726-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (61919-726-90)
Product NDC61919-726
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190215
Marketing Category NameANDA
Application NumberANDA076704
ManufacturerDIRECT RX
Substance NameMETOPROLOL TARTRATE
Strength50
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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