"49999-918-30" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (49999-918-30)
(Lake Erie Medical DBA Quality Care Products LLC)

NDC Code49999-918-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (49999-918-30)
Product NDC49999-918
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20000207
Marketing Category NameANDA
Application NumberANDA075584
ManufacturerLake Erie Medical DBA Quality Care Products LLC
Substance NameBUPROPION HYDROCHLORIDE
Strength75
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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