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
- 63187-692_51ba5811-a7f6-4c07-abde-873a75ba5554
- Product NDC
- 63187-692
- Form
- TABLET, COATED
- Composition / generic term
- MONTELUKAST SODIUM
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20151110
- Source listing expiry
- 20261231
Source-listed ingredients
- MONTELUKAST SODIUM — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, COATED in 1 BOTTLE (63187-692-30) · 63187-692-30
- 60 TABLET, COATED in 1 BOTTLE (63187-692-60) · 63187-692-60
- 90 TABLET, COATED in 1 BOTTLE (63187-692-90) · 63187-692-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →