"61786-380-02" National Drug Code (NDC)

NDC Code	61786-380-02
Package Description	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (61786-380-02)
Product NDC	61786-380
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Bupropion
Non-Proprietary Name	Bupropion
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20150728
Marketing Category Name	ANDA
Application Number	ANDA201567
Manufacturer	REMEDYREPACK INC.
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]