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Desloratadine - 0781-5226-64 - (Desloratadine)

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Drug Information of Desloratadine

Product NDC: 0781-5226
Proprietary Name: Desloratadine
Non Proprietary Name: Desloratadine
Active Ingredient(s): 5    mg/1 & nbsp;   Desloratadine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Desloratadine

Product NDC: 0781-5226
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078364
Marketing Category: ANDA
Start Marketing Date: 20130701

Package Information of Desloratadine

Package NDC: 0781-5226-64
Package Description: 3 BLISTER PACK in 1 CARTON (0781-5226-64) > 10 TABLET in 1 BLISTER PACK

NDC Information of Desloratadine

NDC Code 0781-5226-64
Proprietary Name Desloratadine
Package Description 3 BLISTER PACK in 1 CARTON (0781-5226-64) > 10 TABLET in 1 BLISTER PACK
Product NDC 0781-5226
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desloratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130701
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name DESLORATADINE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of Desloratadine


General Information