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
71205-128_03b5d63d-1c2c-41db-8111-2dcf7e66f010
Product NDC
71205-128
Form
TABLET, CHEWABLE
Composition / generic term
MONTELUKAST
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20150813
Source listing expiry
20261231

Source-listed ingredients

  • MONTELUKAST SODIUM — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, CHEWABLE in 1 BOTTLE (71205-128-30) · 71205-128-30
  • 60 TABLET, CHEWABLE in 1 BOTTLE (71205-128-60) · 71205-128-60
  • 90 TABLET, CHEWABLE in 1 BOTTLE (71205-128-90) · 71205-128-90

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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