"0615-6584-39" National Drug Code (NDC)

Carvedilol 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-6584-39)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-6584-39
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (0615-6584-39)
Product NDC0615-6584
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070905
Marketing Category NameANDA
Application NumberANDA078227
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameCARVEDILOL
Strength6.25
Strength Unitmg/1
Pharmacy ClassesAdrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC]

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