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"0527-2415-32" National Drug Code (NDC)

Bupropion Hydrochloride (xl) 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2415-32)
(Lannett Company Inc.)

NDC Code0527-2415-32
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2415-32)
Product NDC0527-2415
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride (xl)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180108
Marketing Category NameANDA
Application NumberANDA208652
ManufacturerLannett Company 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/0527-2415-32





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