# Montelukast

NDC: 0781-5560
Generic name: Montelukast
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120803

FDA application: ANDA200889

## Active ingredients

- MONTELUKAST SODIUM: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-5560"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-5560
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6d69e73a-76cb-4ece-9cf9-e9adb4f523b4