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Clarinex-D 12 Hour - 54868-5708-0 - (desloratadine and pseudoephedrine sulfate)

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Drug Information of Clarinex-D 12 Hour

Product NDC: 54868-5708
Proprietary Name: Clarinex-D 12 Hour
Non Proprietary Name: desloratadine and pseudoephedrine sulfate
Active Ingredient(s): 2.5; 120    mg/1; mg/1 & nbsp;   desloratadine and pseudoephedrine sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Clarinex-D 12 Hour

Product NDC: 54868-5708
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021313
Marketing Category: NDA
Start Marketing Date: 20061129

Package Information of Clarinex-D 12 Hour

Package NDC: 54868-5708-0
Package Description: 10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5708-0)

NDC Information of Clarinex-D 12 Hour

NDC Code 54868-5708-0
Proprietary Name Clarinex-D 12 Hour
Package Description 10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5708-0)
Product NDC 54868-5708
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name desloratadine and pseudoephedrine sulfate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20061129
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name DESLORATADINE; PSEUDOEPHEDRINE SULFATE
Strength Number 2.5; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]

Complete Information of Clarinex-D 12 Hour


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