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"61919-726-82" National Drug Code (NDC)

Metoprolol Tartrate 180 TABLET, FILM COATED in 1 BOTTLE (61919-726-82)
(Direct_Rx)

NDC Code61919-726-82
Package Description180 TABLET, FILM COATED in 1 BOTTLE (61919-726-82)
Product NDC61919-726
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190821
Marketing Category NameANDA
Application NumberANDA076704
ManufacturerDirect_Rx
Substance NameMETOPROLOL TARTRATE
Strength50
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-726-82





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