Astelin - 0037-0241-05 - (Azelastine Hydrochloride)

Alphabetical Index


Drug Information of Astelin

Product NDC: 0037-0241
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: 0037-0241
Labeler Name: Meda Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020114
Marketing Category: NDA
Start Marketing Date: 19961115

Package Information of Astelin

Package NDC: 0037-0241-05
Package Description: 1 BOTTLE, SPRAY in 1 BOX (0037-0241-05) > 16 SPRAY, METERED in 1 BOTTLE, SPRAY

NDC Information of Astelin

NDC Code 0037-0241-05
Proprietary Name Astelin
Package Description 1 BOTTLE, SPRAY in 1 BOX (0037-0241-05) > 16 SPRAY, METERED in 1 BOTTLE, SPRAY
Product NDC 0037-0241
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azelastine Hydrochloride
Dosage Form Name SPRAY, METERED
Route Name NASAL
Start Marketing Date 19961115
Marketing Category Name NDA
Labeler Name Meda Pharmaceuticals 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