"0615-7904-39" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-7904-39)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-7904-39
Package Description30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-7904-39)
Product NDC0615-7904
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixSr
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20040322
Marketing Category NameANDA
Application NumberANDA075932
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameBUPROPION HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesAminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]

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