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AZELASTINE HYDROCHLORIDE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARM · Approved 2010-06-21

Drug application

FDA Application #

ANDA078738

Application type

Abbreviated New Drug Application (Generic)

Brand name

AZELASTINE HYDROCHLORIDE

Generic name

AZELASTINE HYDROCHLORIDE

Active ingredients

AZELASTINE HYDROCHLORIDE

Dosage form

SOLUTION/DROPS

Route

OPHTHALMIC

Marketing status

Discontinued

Sponsor

SUN PHARM

Manufacturer

Sun Pharmaceutical Industries, Inc.

First approval

2010-06-21

Source

Authoritative

Drugs@FDA application overview

Machine

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