# Formoterol fumarate

NDC: 72603-620
Generic name: Formoterol fumarate dihydrate
Labeler / Manufacturer: NorthStar RxLLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20240701

FDA application: ANDA215883

## Active ingredients

- FORMOTEROL FUMARATE: 20 ug/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-620"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-620
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4dbb9620-5731-40d9-8258-2977ecc781c4