"52125-982-02" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (52125-982-02)
(REMEDYREPACK INC.)

NDC Code52125-982-02
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (52125-982-02)
Product NDC52125-982
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20140703
Marketing Category NameANDA
Application NumberANDA077284
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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