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Desloratadine - 76439-107-10 - (Desloratadine)

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Drug Information of Desloratadine

Product NDC: 76439-107
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: 76439-107
Labeler Name: Virtus Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078355
Marketing Category: ANDA
Start Marketing Date: 20120701

Package Information of Desloratadine

Package NDC: 76439-107-10
Package Description: 100 TABLET in 1 BOTTLE (76439-107-10)

NDC Information of Desloratadine

NDC Code 76439-107-10
Proprietary Name Desloratadine
Package Description 100 TABLET in 1 BOTTLE (76439-107-10)
Product NDC 76439-107
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desloratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120701
Marketing Category Name ANDA
Labeler Name Virtus Pharmaceuticals
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


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