Home > National Drug Code (NDC) > Desloratadine

Desloratadine - 16714-339-02 - (Desloratadine)

Alphabetical Index


Drug Information of Desloratadine

Product NDC: 16714-339
Proprietary Name: Desloratadine
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 Desloratadine

Product NDC: 16714-339
Labeler Name: Northstar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078357
Marketing Category: ANDA
Start Marketing Date: 20130116

Package Information of Desloratadine

Package NDC: 16714-339-02
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-339-02)

NDC Information of Desloratadine

NDC Code 16714-339-02
Proprietary Name Desloratadine
Package Description 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-339-02)
Product NDC 16714-339
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desloratadine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130116
Marketing Category Name ANDA
Labeler Name Northstar Rx 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


General Information