# Montelukast Sodium

NDC: 13668-080
Generic name: Montelukast Sodium
Labeler / Manufacturer: Torrent Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, CHEWABLE
Routes: ORAL
Marketing started: 20120803

FDA application: ANDA090984

## Active ingredients

- MONTELUKAST SODIUM: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"13668-080"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13668-080
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=da038cf6-cfad-43a4-ab8e-d81d028d6087