"31722-068-90" National Drug Code (NDC)

NDC Code	31722-068-90
Package Description	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-90)
Product NDC	31722-068
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Bupropion Hydrochloride
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20230531
Marketing Category Name	ANDA
Application Number	ANDA216800
Manufacturer	Camber Pharmaceuticals, Inc.
Substance Name	BUPROPION HYDROCHLORIDE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]