Claritin - 11523-7237-1 - (Loratadine)

Alphabetical Index


Drug Information of Claritin

Product NDC: 11523-7237
Proprietary Name: Claritin
Non Proprietary Name: Loratadine
Active Ingredient(s): 10    mg/1 & nbsp;   Loratadine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Claritin

Product NDC: 11523-7237
Labeler Name: MSD Consumer Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA019658
Marketing Category: NDA
Start Marketing Date: 19930412

Package Information of Claritin

Package NDC: 11523-7237-1
Package Description: 1 BOTTLE in 1 CARTON (11523-7237-1) > 45 TABLET in 1 BOTTLE

NDC Information of Claritin

NDC Code 11523-7237-1
Proprietary Name Claritin
Package Description 1 BOTTLE in 1 CARTON (11523-7237-1) > 45 TABLET in 1 BOTTLE
Product NDC 11523-7237
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930412
Marketing Category Name NDA
Labeler Name MSD Consumer Care, Inc.
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Claritin


General Information