Claritin - 11523-7197-3 - (loratadine)

Alphabetical Index


Drug Information of Claritin

Product NDC: 11523-7197
Proprietary Name: Claritin
Non Proprietary Name: loratadine
Active Ingredient(s): 5    mg/5mL & nbsp;   loratadine
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Claritin

Product NDC: 11523-7197
Labeler Name: MSD Consumer Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020641
Marketing Category: NDA
Start Marketing Date: 20110301

Package Information of Claritin

Package NDC: 11523-7197-3
Package Description: 1 BOTTLE in 1 CARTON (11523-7197-3) > 20 mL in 1 BOTTLE

NDC Information of Claritin

NDC Code 11523-7197-3
Proprietary Name Claritin
Package Description 1 BOTTLE in 1 CARTON (11523-7197-3) > 20 mL in 1 BOTTLE
Product NDC 11523-7197
Product Type Name HUMAN OTC DRUG
Non Proprietary Name loratadine
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20110301
Marketing Category Name NDA
Labeler Name MSD Consumer Care, Inc.
Substance Name LORATADINE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Claritin


General Information