United States · FDA National Drug Code directory
Montelukast
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
- 33342-102_c0c72c6c-cc59-47ba-9dfb-0af985ae7ea6
- Product NDC
- 33342-102
- Form
- TABLET
- Composition / generic term
- Montelukast
- Labeler
- Macleods Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140911
- 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 in 1 BOTTLE (33342-102-07) · 33342-102-07
- 90 TABLET in 1 BOTTLE (33342-102-10) · 33342-102-10
- 100 TABLET in 1 BLISTER PACK (33342-102-12) · 33342-102-12
- 500 TABLET in 1 BOTTLE (33342-102-15) · 33342-102-15
- 90 TABLET in 1 BLISTER PACK (33342-102-39) · 33342-102-39
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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