United States · FDA National Drug Code directory

Ketotifen Fumarate

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
50090-6472_9b869ed6-cd2a-48b5-84b1-c5e0e1f29a89
Product NDC
50090-6472
Form
SOLUTION/ DROPS
Composition / generic term
Ketotifen Fumarate
Labeler
A-S Medication Solutions
Marketing category
NDA AUTHORIZED GENERIC
Marketing start / end (source format)
20200918
Source listing expiry
20261231

Source-listed ingredients

  • KETOTIFEN FUMARATE — .25 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, DROPPER in 1 CARTON (50090-6472-0) / 5 mL in 1 BOTTLE, DROPPER · 50090-6472-0

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Ketotifen Fumarate — United States | Molindra Medicines