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"0781-5169-60" National Drug Code (NDC)

Bupropion Hydrochloride 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5169-60)
(Sandoz Inc)

NDC Code0781-5169-60
Package Description60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5169-60)
Product NDC0781-5169
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20080312
Marketing Category NameANDA
Application NumberANDA077475
ManufacturerSandoz 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/0781-5169-60





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