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"72516-035-09" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-035-09)
(Oryza pharmaceuticals Inc.)

NDC Code72516-035-09
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-035-09)
Product NDC72516-035
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixXl
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20201001
Marketing Category NameANDA
Application NumberANDA211200
ManufacturerOryza pharmaceuticals 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/72516-035-09





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