Claritin-D - 11523-7161-1 - (Loratadine and pseudoephedrine sulfate)

Alphabetical Index


Drug Information of Claritin-D

Product NDC: 11523-7161
Proprietary Name: Claritin-D
Non Proprietary Name: Loratadine and pseudoephedrine sulfate
Active Ingredient(s): 10; 240    mg/1; mg/1 & nbsp;   Loratadine and pseudoephedrine sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Claritin-D

Product NDC: 11523-7161
Labeler Name: MSD Consumer Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020470
Marketing Category: NDA
Start Marketing Date: 20091201

Package Information of Claritin-D

Package NDC: 11523-7161-1
Package Description: 1 BLISTER PACK in 1 CARTON (11523-7161-1) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Claritin-D

NDC Code 11523-7161-1
Proprietary Name Claritin-D
Package Description 1 BLISTER PACK in 1 CARTON (11523-7161-1) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 11523-7161
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine and pseudoephedrine sulfate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20091201
Marketing Category Name NDA
Labeler Name MSD Consumer Care, Inc.
Substance Name LORATADINE; PSEUDOEPHEDRINE SULFATE
Strength Number 10; 240
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Claritin-D


General Information