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"61919-063-72" National Drug Code (NDC)

Bupropion Hydrochloride 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-063-72)
(DIRECT RX)

NDC Code61919-063-72
Package Description120 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-063-72)
Product NDC61919-063
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20170216
Marketing Category NameANDA
Application NumberANDA075932
ManufacturerDIRECT RX
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-063-72





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