"49349-704-02" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET in 1 BLISTER PACK (49349-704-02)
(REMEDYREPACK INC.)

NDC Code49349-704-02
Package Description30 TABLET in 1 BLISTER PACK (49349-704-02)
Product NDC49349-704
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20110912
Marketing Category NameANDA
Application NumberANDA075310
ManufacturerREMEDYREPACK INC.
Substance NameBUPROPION HYDROCHLORIDE
Strength100
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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