"0363-0522-56" National Drug Code (NDC)

NDC Code	0363-0522-56
Package Description	1 BLISTER PACK in 1 CARTON (0363-0522-56) > 5 TABLET in 1 BLISTER PACK
Product NDC	0363-0522
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Loratadine
Non-Proprietary Name	Loratadine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20131205
Marketing Category Name	ANDA
Application Number	ANDA076134
Manufacturer	Walgreen Company
Substance Name	LORATADINE
Strength	10
Strength Unit	mg/1