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"71335-2652-7" National Drug Code (NDC)

Bupropion Hydrochloride 21 TABLET, FILM COATED in 1 BOTTLE (71335-2652-7)
(Bryant Ranch Prepack)

NDC Code71335-2652-7
Package Description21 TABLET, FILM COATED in 1 BOTTLE (71335-2652-7)
Product NDC71335-2652
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240425
Marketing Category NameANDA
Application NumberANDA075491
ManufacturerBryant Ranch Prepack
Substance NameBUPROPION HYDROCHLORIDE
Strength100
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/71335-2652-7





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