"0904-7214-61" National Drug Code (NDC)

NDC Code	0904-7214-61
Package Description	100 BLISTER PACK in 1 CARTON (0904-7214-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC	0904-7214
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Bupropion Hydrochloride
Proprietary Name Suffix	Sr
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20220707
End Marketing Date	20250430
Marketing Category Name	ANDA
Application Number	ANDA211347
Manufacturer	Major Pharmaceuticals
Substance Name	BUPROPION HYDROCHLORIDE
Strength	150
Strength Unit	mg/1
Pharmacy Classes	Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]