Astelin - 54868-5072-0 - (Azelastine Hydrochloride)

Alphabetical Index


Drug Information of Astelin

Product NDC: 54868-5072
Proprietary Name: Astelin
Non Proprietary Name: Azelastine Hydrochloride
Active Ingredient(s): 137    ug/1 & nbsp;   Azelastine Hydrochloride
Administration Route(s): NASAL
Dosage Form(s): SPRAY, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of Astelin

Product NDC: 54868-5072
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020114
Marketing Category: NDA
Start Marketing Date: 20040525

Package Information of Astelin

Package NDC: 54868-5072-0
Package Description: 1 BOTTLE, SPRAY in 1 BOX (54868-5072-0) > 200 SPRAY, METERED in 1 BOTTLE, SPRAY

NDC Information of Astelin

NDC Code 54868-5072-0
Proprietary Name Astelin
Package Description 1 BOTTLE, SPRAY in 1 BOX (54868-5072-0) > 200 SPRAY, METERED in 1 BOTTLE, SPRAY
Product NDC 54868-5072
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azelastine Hydrochloride
Dosage Form Name SPRAY, METERED
Route Name NASAL
Start Marketing Date 20040525
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name AZELASTINE HYDROCHLORIDE
Strength Number 137
Strength Unit ug/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC]

Complete Information of Astelin


General Information