"41163-528-69" National Drug Code (NDC)

NDC Code	41163-528-69
Package Description	1 BLISTER PACK in 1 CARTON (41163-528-69) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC	41163-528
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Loratadine
Non-Proprietary Name	Loratadine
Dosage Form	TABLET, ORALLY DISINTEGRATING
Usage	ORAL
Start Marketing Date	20131203
Marketing Category Name	ANDA
Application Number	ANDA077153
Manufacturer	Supervalu Inc.
Substance Name	LORATADINE
Strength	10
Strength Unit	mg/1