# Montelukast Sodium

NDC: 57237-255
Generic name: Montelukast Sodium
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120803

FDA application: ANDA202468

## 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:"57237-255"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57237-255
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=49669ac0-0bb5-4576-bed5-9e85e0d76a44