"85534-0006-3" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-3)
(HAWAII REPACK, INC.)

NDC Code85534-0006-3
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-3)
Product NDC85534-0006
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20150217
Marketing Category NameANDA
Application NumberANDA077285
ManufacturerHAWAII REPACK, INC.
Substance NameBUPROPION HYDROCHLORIDE
Strength300
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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