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"70518-0639-0" National Drug Code (NDC)

Wellbutrin 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0639-0)
(REMEDYREPACK INC.)

NDC Code70518-0639-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0639-0)
Product NDC70518-0639
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameWellbutrin
Proprietary Name SuffixSr
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170725
Marketing Category NameNDA
Application NumberNDA020358
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0639-0





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