"11523-7160-1" National Drug Code (NDC)

NDC Code	11523-7160-1
Package Description	1 BLISTER PACK in 1 CARTON (11523-7160-1) > 5 TABLET in 1 BLISTER PACK
Product NDC	11523-7160
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Claritin
Non-Proprietary Name	Loratadine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19930412
Marketing Category Name	NDA
Application Number	NDA019658
Manufacturer	Bayer HealthCare LLC.
Substance Name	LORATADINE
Strength	10
Strength Unit	mg/1