Claritin - 11523-7202-1 - (Loratadine)

Alphabetical Index


Drug Information of Claritin

Product NDC: 11523-7202
Proprietary Name: Claritin
Non Proprietary Name: Loratadine
Active Ingredient(s): 5    mg/1 & nbsp;   Loratadine
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Claritin

Product NDC: 11523-7202
Labeler Name: MSD Consumer Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021993
Marketing Category: NDA
Start Marketing Date: 20061212

Package Information of Claritin

Package NDC: 11523-7202-1
Package Description: 3 BLISTER PACK in 1 CARTON (11523-7202-1) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Claritin

NDC Code 11523-7202-1
Proprietary Name Claritin
Package Description 3 BLISTER PACK in 1 CARTON (11523-7202-1) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 11523-7202
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20061212
Marketing Category Name NDA
Labeler Name MSD Consumer Care, Inc.
Substance Name LORATADINE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Claritin


General Information