"72189-539-90" National Drug Code (NDC)

NDC Code	72189-539-90
Package Description	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-539-90)
Product NDC	72189-539
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Bupropion Hcl Er (xl)
Non-Proprietary Name	Bupropion Hcl Er (xl)
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20240301
Marketing Category Name	ANDA
Application Number	ANDA210015
Manufacturer	Direct_RX
Substance Name	BUPROPION HYDROCHLORIDE
Strength	300
Strength Unit	mg/1
Pharmacy Classes	Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]