"68084-002-21" National Drug Code (NDC)

NDC Code	68084-002-21
Package Description	30 BLISTER PACK in 1 CARTON (68084-002-21) > 1 CAPSULE in 1 BLISTER PACK (68084-002-11)
Product NDC	68084-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Loxapine
Non-Proprietary Name	Loxapine
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20130415
End Marketing Date	20180131
Marketing Category Name	ANDA
Application Number	ANDA090695
Manufacturer	American Health Packaging
Substance Name	LOXAPINE SUCCINATE
Strength	10
Strength Unit	mg/1