"0378-0636-88" National Drug Code (NDC)

NDC Code	0378-0636-88
Package Description	10 BLISTER PACK in 1 CARTON (0378-0636-88) > 10 TABLET in 1 BLISTER PACK
Product NDC	0378-0636
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Iloperidone
Non-Proprietary Name	Iloperidone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20170320
Marketing Category Name	ANDA
Application Number	ANDA207231
Manufacturer	Mylan Pharmaceuticals Inc.
Substance Name	ILOPERIDONE
Strength	12
Strength Unit	mg/1
Pharmacy Classes	Atypical Antipsychotic [EPC]