"49349-230-02" National Drug Code (NDC)

Bupropion Hydrocloride 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-230-02)
(REMEDYREPACK INC.)

NDC Code49349-230-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (49349-230-02)
Product NDC49349-230
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrocloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110314
Marketing Category NameANDA
Application NumberANDA075584
ManufacturerREMEDYREPACK INC.
Substance NameBUPROPION HYDROCHLORIDE
Strength75
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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