"0615-8017-39" National Drug Code (NDC)

Metoprolol Tartrate 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8017-39)
(NCS HealthCare of KY, LLC dba Vangard Labs)

NDC Code0615-8017-39
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8017-39)
Product NDC0615-8017
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19931223
End Marketing Date20231130
Marketing Category NameANDA
Application NumberANDA076704
ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Substance NameMETOPROLOL TARTRATE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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