"70518-1711-1" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1711-1)
(REMEDYREPACK INC.)

NDC Code70518-1711-1
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1711-1)
Product NDC70518-1711
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20181206
Marketing Category NameANDA
Application NumberANDA090693
ManufacturerREMEDYREPACK 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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