"51079-392-20" National Drug Code (NDC)

Bupropion Hydrochloride 100 BLISTER PACK in 1 CARTON (51079-392-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-392-01)
(Mylan Institutional Inc.)

NDC Code51079-392-20
Package Description100 BLISTER PACK in 1 CARTON (51079-392-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-392-01)
Product NDC51079-392
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20100528
End Marketing Date20191031
Marketing Category NameANDA
Application NumberANDA090325
ManufacturerMylan Institutional Inc.
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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