# Alaway

NDC: 24208-601
Generic name: Ketotifen Fumarate
Labeler / Manufacturer: Bausch & Lomb Incorporated
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20061201

FDA application: NDA021996

## Active ingredients

- KETOTIFEN FUMARATE: .25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24208-601"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24208-601
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e4c310b5-1dba-4ddc-bc90-b27ebc765871