"68084-431-21" National Drug Code (NDC)

NDC Code	68084-431-21
Package Description	3 BLISTER PACK in 1 CARTON (68084-431-21) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (68084-431-11)
Product NDC	68084-431
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Didanosine
Non-Proprietary Name	Didanosine
Dosage Form	CAPSULE, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	20091208
Marketing Category Name	ANDA
Application Number	ANDA077167
Manufacturer	American Health Packaging
Substance Name	DIDANOSINE
Strength	250
Strength Unit	mg/1
Pharmacy Classes	Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]