# Montelukast Sodium

NDC: 16729-119
Generic name: Montelukast Sodium
Labeler / Manufacturer: Accord Healthcare Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20130411

FDA application: ANDA202717

## Active ingredients

- MONTELUKAST SODIUM: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16729-119"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16729-119
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6eea668f-a2fa-447f-b2d5-4c754d13d9fa