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"0781-5529-10" National Drug Code (NDC)

Bupropion Hydrochloride (xl) 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5529-10)
(Sandoz Inc.)

NDC Code0781-5529-10
Package Description1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5529-10)
Product NDC0781-5529
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride (xl)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180108
End Marketing Date20230531
Marketing Category NameANDA
Application NumberANDA208652
ManufacturerSandoz 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/0781-5529-10





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