# MONTELUKAST SODIUM

NDC: 63187-751
Generic name: MONTELUKAST SODIUM
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, CHEWABLE
Routes: ORAL
Marketing started: 20151110

FDA application: ANDA203328

## Active ingredients

- MONTELUKAST SODIUM: 4 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63187-751"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63187-751
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=54014b67-3163-4c8f-b93a-229cd231ca6b