Azelastine Hydrochloride

Product NDC

50090-2538

11-digit product format

500902538

Labeler code

50090

Product ID

50090-2538_9413391f-b54d-40cb-9c2a-5772484886b9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Azelastine Hydrochloride

Dosage form

SPRAY, METERED

Route

NASAL

Labeler

A-S Medication Solutions

Application

NDA020114

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2010-07-01

Marketing end

0000-00-00

Substance

AZELASTINE HYDROCHLORIDE

Active strength

137 ug/1

Pharmacologic classes

Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record