Eye Itch Relief

Product NDC

50804-302

11-digit product format

508040302

Labeler code

50804

Product ID

50804-302_26dcbffe-cdc5-4f58-a056-b1405504eb05

Type

HUMAN OTC DRUG

Nonproprietary name

Ketotifen Fumarate

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

Good Sense

Application

ANDA077958

Marketing category

ANDA

Marketing start

2014-06-20

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