"61919-705-60" National Drug Code (NDC)

Metoprolol Tartrate 60 TABLET, FILM COATED in 1 BOTTLE (61919-705-60)
(Direct_Rx)

NDC Code61919-705-60
Package Description60 TABLET, FILM COATED in 1 BOTTLE (61919-705-60)
Product NDC61919-705
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190719
Marketing Category NameANDA
Application NumberANDA077739
ManufacturerDirect_Rx
Substance NameMETOPROLOL TARTRATE
Strength25
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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