Clarinex - 21695-815-10 - (Desloratadine)

Alphabetical Index


Drug Information of Clarinex

Product NDC: 21695-815
Proprietary Name: Clarinex
Non Proprietary Name: Desloratadine
Active Ingredient(s): 5    mg/1 & nbsp;   Desloratadine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Clarinex

Product NDC: 21695-815
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021297
Marketing Category: NDA
Start Marketing Date: 20020208

Package Information of Clarinex

Package NDC: 21695-815-10
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE (21695-815-10)

NDC Information of Clarinex

NDC Code 21695-815-10
Proprietary Name Clarinex
Package Description 10 TABLET, FILM COATED in 1 BOTTLE (21695-815-10)
Product NDC 21695-815
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desloratadine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020208
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
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 Clarinex


General Information