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"61919-037-30" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (61919-037-30)
(DirectRX)

NDC Code61919-037-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (61919-037-30)
Product NDC61919-037
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20151125
Marketing Category NameANDA
Application NumberANDA075584
ManufacturerDirectRX
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-037-30





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