"61919-052-82" National Drug Code (NDC)

Metoprolol Tartrate 180 TABLET in 1 BOTTLE (61919-052-82)
(DIRECT RX)

NDC Code61919-052-82
Package Description180 TABLET in 1 BOTTLE (61919-052-82)
Product NDC61919-052
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA076670
ManufacturerDIRECT RX
Substance NameMETOPROLOL TARTRATE
Strength25
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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