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Desloratadine - 55111-360-31 - (Desloratadine)

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Drug Information of Desloratadine

Product NDC: 55111-360
Proprietary Name: Desloratadine
Non Proprietary Name: Desloratadine
Active Ingredient(s): 5    mg/1 & nbsp;   Desloratadine
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Desloratadine

Product NDC: 55111-360
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078367
Marketing Category: ANDA
Start Marketing Date: 20130111

Package Information of Desloratadine

Package NDC: 55111-360-31
Package Description: 5 BLISTER PACK in 1 CARTON (55111-360-31) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (55111-360-06)

NDC Information of Desloratadine

NDC Code 55111-360-31
Proprietary Name Desloratadine
Package Description 5 BLISTER PACK in 1 CARTON (55111-360-31) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (55111-360-06)
Product NDC 55111-360
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desloratadine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20130111
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
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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