United States · FDA National Drug Code directory

MONTELUKAST SODIUM

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
72189-223_2c283d75-2454-ee48-e063-6294a90a7651
Product NDC
72189-223
Form
TABLET, CHEWABLE
Composition / generic term
MONTELUKAST SODIUM
Labeler
DIRECT RX
Marketing category
ANDA
Marketing start / end (source format)
20210521
Source listing expiry
20261231

Source-listed ingredients

  • MONTELUKAST — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, CHEWABLE in 1 BOTTLE (72189-223-30) · 72189-223-30

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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