"72065-002-01" National Drug Code (NDC)

NDC Code	72065-002-01
Package Description	100 TABLET in 1 BOTTLE (72065-002-01)
Product NDC	72065-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Dichlorphenamide
Non-Proprietary Name	Dichlorphenamide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20230310
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA011366
Manufacturer	Xeris Pharmaceuticals, Inc.
Substance Name	DICHLORPHENAMIDE
Strength	50
Strength Unit	mg/1
Pharmacy Classes	Carbonic Anhydrase Inhibitor [EPC], Carbonic Anhydrase Inhibitors [MoA], Sulfonamides [CS]