"61919-558-72" National Drug Code (NDC)

NDC Code	61919-558-72
Package Description	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-558-72)
Product NDC	61919-558
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	20240215
Marketing Category Name	ANDA
Application Number	ANDA090693
Manufacturer	Direct_Rx
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]