"0615-8504-39" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8504-39)
(NCS HealthCare of KY, LLC dba Vangard Labs)

NDC Code0615-8504-39
Package Description30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8504-39)
Product NDC0615-8504
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20220801
Marketing Category NameANDA
Application NumberANDA211020
ManufacturerNCS HealthCare of KY, LLC 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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