"70518-2022-0" National Drug Code (NDC)

Bupropion Hydrochloride 30 POUCH in 1 BOX (70518-2022-0) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-2022-1)
(REMEDYREPACK INC.)

NDC Code70518-2022-0
Package Description30 POUCH in 1 BOX (70518-2022-0) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-2022-1)
Product NDC70518-2022
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20190415
Marketing Category NameANDA
Application NumberANDA090693
ManufacturerREMEDYREPACK 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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