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"61786-073-02" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61786-073-02)
(REMEDYREPACK INC.)

NDC Code61786-073-02
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61786-073-02)
Product NDC61786-073
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20141230
Marketing Category NameANDA
Application NumberANDA077285
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61786-073-02





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