Eye Itch Relief

Product NDC

49781-075

11-digit product format

497810075

Labeler code

49781

Product ID

49781-075_b8c16af4-16f0-498b-8f3e-3c6f7f1edf48

Type

HUMAN OTC DRUG

Nonproprietary name

Ketotifen Fumarate

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

Cardinal Health

Application

ANDA077958

Marketing category

ANDA

Marketing start

2014-01-13

Marketing end

0000-00-00

Substance

KETOTIFEN FUMARATE

Active strength

0 mg/mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record