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"71335-0612-7" National Drug Code (NDC)

Bupropion Hydrochloride 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0612-7)
(Bryant Ranch Prepack)

NDC Code71335-0612-7
Package Description28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0612-7)
Product NDC71335-0612
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20040322
Marketing Category NameANDA
Application NumberANDA075932
ManufacturerBryant Ranch Prepack
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/71335-0612-7





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