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"71335-2378-5" National Drug Code (NDC)

Bupropion Hydrochloride 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-5)
(Bryant Ranch Prepack)

NDC Code71335-2378-5
Package Description14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-5)
Product NDC71335-2378
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixXl
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20230430
Marketing Category NameANDA
Application NumberANDA210015
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/71335-2378-5





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