# montelukast sodium

NDC: 29300-220
Generic name: montelukast sodium
Labeler / Manufacturer: Unichem Pharmaceuticals (USA), Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160101

FDA application: ANDA204290

## 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:"29300-220"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=29300-220
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9e375c07-70db-458c-9336-22a7037b0a5f