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"70518-1229-1" National Drug Code (NDC)

Bupropion Hydrochloride (xl) 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1229-1)
(REMEDYREPACK INC.)

NDC Code70518-1229-1
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1229-1)
Product NDC70518-1229
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride (xl)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180525
Marketing Category NameANDA
Application NumberANDA208652
ManufacturerREMEDYREPACK INC.
Substance NameBUPROPION HYDROCHLORIDE
Strength300
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/70518-1229-1





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