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Desloratadine - 62250-619-01 - (Desloratadine)

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Drug Information of Desloratadine

Product NDC: 62250-619
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: 62250-619
Labeler Name: Belcher Pharmaceuticals,LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078355
Marketing Category: ANDA
Start Marketing Date: 20120515

Package Information of Desloratadine

Package NDC: 62250-619-01
Package Description: 30 TABLET in 1 BOTTLE (62250-619-01)

NDC Information of Desloratadine

NDC Code 62250-619-01
Proprietary Name Desloratadine
Package Description 30 TABLET in 1 BOTTLE (62250-619-01)
Product NDC 62250-619
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desloratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120515
Marketing Category Name ANDA
Labeler Name Belcher Pharmaceuticals,LLC
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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