Eye Itch Relief (ketotifen fumarate) NDC 70000-0522

Product information

Brand name (proprietary)

Eye Itch Relief

Generic name (nonproprietary)

ketotifen fumarate

Active ingredients

Ketotifen fumarate — .25 mg/mL

Dosage form

Solution

Route

Ophthalmic

Labeler

Cardinal Health

Product type

Over-the-counter drug

Marketing category

NDA — New Drug ApplicationApplication NDA 021996

Marketing start

Aug 7, 2020

Listing expires

Dec 31, 2026

Other FDA classes

Histamine H1 Receptor Antagonists (Mechanism)

Identifiers

Product ID 70000-0522_5f7ef9e0-7c0a-4e3e-b943-e1b47e3e2623SPL ID 5f7ef9e0-7c0a-4e3e-b943-e1b47e3e2623SPL set ID e5fd1246-c4a7-4be3-a3d3-83d82ec6cab8RxCUI 311237UNII HBD503WOROUPC 0096295138887

Pharmacologic class

Histamine-1 Receptor Inhibitor

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470000052201 followed by a unit qualifier and the quantity Copy

Package 70000-0522-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Other NDCs under NDA 021996

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.