"0781-2322-68" National Drug Code (NDC)

NDC Code	0781-2322-68
Package Description	1 BLISTER PACK in 1 CARTON (0781-2322-68) / 6 CAPSULE in 1 BLISTER PACK (0781-2322-06)
Product NDC	0781-2322
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Aprepitant
Non-Proprietary Name	Aprepitant
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20161227
Marketing Category Name	ANDA
Application Number	ANDA090999
Manufacturer	Sandoz Inc
Substance Name	APREPITANT
Strength	80
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 3A4 Inducers [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Neurokinin 1 Antagonists [MoA], Substance P/Neurokinin-1 Receptor Antagonist [EPC]