Montelukast
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Montelukast
- Generic name
- MONTELUKAST
- Manufacturer
- NuCare Pharmaceuticals,Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 56429f04-97b6-06a9-e054-00144ff88e88
- SPL ID
- 1d7a445a-3c64-0235-e063-6394a90add16
- Version
- 4
- Effective date
- 2024-07-17
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:53:22
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 203366 | derived:openfda.application_number |
| application number | ANDA203366 | openfda.application_number | |
| brand name | Montelukast | openfda.brand_name | |
| generic name | MONTELUKAST | openfda.generic_name | |
| manufacturer name | NuCare Pharmaceuticals,Inc. | openfda.manufacturer_name | |
| ndc | package | 68071-4034-9 | openfda.package_ndc |
| ndc | product | 68071-4034 | openfda.product_ndc |
| ndc11 | package | 68071403409 | derived:openfda.package_ndc |
| rxcui | 200224 | openfda.rxcui | |
| spl id | 1d7a445a-3c64-0235-e063-6394a90add16 | id | |
| spl set id | 56429f04-97b6-06a9-e054-00144ff88e88 | set_id | |
| unii | U1O3J18SFL | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
5 WARNINGS AND PRECAUTIONS Do not prescribe montelukast sodium to treat an acute asthma attack. Advise patients to have appropriate rescue medication available ( 5.1 ). Inhaled corticosteroid may be reduced gradually. Do not abruptly substitute montelukast sodium for inhaled or oral corticosteroids ( 5.2 ). Patients with known aspirin sensitivity should continue to avoid aspirin or non-steroidal anti-inflammatory agents while taking montelukast sodium( 5.3 ). Neuropsychiatric events have been reported with montelukast sodium. Instruct patients to be alert for neuropsychiatric events. Evaluate the risks and benefits of continuing treatment with montelukast sodium if such events occur ( 5.4 and 6.2 ). Systemic eosinophilia, sometimes presenting with clinical features of vasculitis consistent with Churg-Strauss syndrome, has been reported. These events have been sometimes associated with the reduction of oral corticosteroid therapy ( 5.5 and 6.2 ). 5.1 Acute Asthma Montelukast sodium is not indicated for use in the reversal of bronchospasm in acute asthma attacks, including status asthmaticus. Patients should be advised to have appropriate rescue medication available. Therapy with montelukast sodium can be continued during acute exacerbations of asthma. Patients who have exacerbations of asthma after exercise should have available for rescue a short-acting inhaled ß-agonist. 5.2 Concomitant Corticosteroid Use While the dose of inhaled corticosteroid may be reduced gradually under medical supervision, montelukast sodium should not be abruptly substituted for inhaled or oral corticosteroids. 5.3 Aspirin Sensitivity Patients with known aspirin sensitivity should continue avoidance of aspirin or non-steroidal anti-inflammatory agents while taking montelukast sodium. Although montelukast sodium is effective in improving airway function in asthmatics with documented aspirin sensitivity, it has not been shown to truncate bronchoconstrictor response to aspirin and other non-steroidal anti-inflammatory drugs in aspirin-sensitive asthmatic patients [see Clinical Studies (14.1 )]. 5.4 Neuropsychiatric Events Patients and prescribers should be alert for neuropsychiatric events. Patients should be instructed to notify their prescriber if these changes occur. Prescribers should carefully evaluate the risks and benefits of continuing treatment with montelukast sodium if such events occur . Neuropsychiatric events have been reported in adult, adolescent, and pediatric patients taking montelukast sodium. Post-marketing reports with montelukast use include agitation, aggressive behavior or hostility, anxiousness, depression, disorientation, disturbance in attention, dream abnormalities, hallucinations, insomnia, irritability, memory impairment, restlessness, somnambulism, suicidal thinking and behavior (including suicide), tic, and tremor. The clinical details of some post-marketing reports involving montelukast sodium appear consistent with a drug-induced effect. Patients and prescribers should be alert for neuropsychiatric events. Patients should be instructed to notify their prescriber if these changes occur. Prescribers should carefully evaluate the risks and benefits of continuing treatment with montelukast sodium if such events occur [see Adverse Reactions (6.2 )] . 5.5 Eosinophilic Conditions Patients with asthma on therapy with montelukast sodium may present with systemic eosinophilia, sometimes presenting with clinical features of vasculitis consistent with Churg-Strauss syndrome, a condition which is often treated with systemic corticosteroid therapy. These events have been sometimes associated with the reduction of oral corticosteroid therapy. Physicians should be alert to eosinophilia, vasculitic rash, worsening pulmonary symptoms, cardiac complications, and/or neuropathy presenting in their patients. A causal association between montelukast sodium and these underlying conditions has not been established [see Adverse Reactions ( 6.2 )].
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
6 ADVERSE REACTIONS Most common adverse reactions (incidence ≥ 5% and greater than placebo listed in descending order of frequency): upper respiratory infection, fever, headache, pharyngitis, cough, abdominal pain, diarrhea, otitis media, influenza, rhinorrhea, sinusitis, otitis ( 6.1 ). To report SUSPECTED ADVERSE REACTIONS, contact Macleods Pharma USA, Inc., at 1-888-943-3210 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice. In the following description of clinical trials experience, adverse reactions are listed regardless of causality assessment. The most common adverse reactions (incidence ≥5% and greater than placebo; listed in descending order of frequency) in controlled clinical trials were: upper respiratory infection, fever, headache, pharyngitis, cough, abdominal pain, diarrhea, otitis media, influenza, rhinorrhea, sinusitis, otitis. Adults and Adolescents 15 Years of Age and Older with Asthma Montelukast sodium has been evaluated for safety in approximately 2950 adult and adolescent patients 15 years of age and older in clinical trials. In placebo-controlled clinical trials, the following adverse experiences reported with montelukast occurred in greater than or equal to 1% of patients and at an incidence greater than that in patients treated with placebo: TABLE 1: Adverse Experiences Occurring in ≥1% of Patients with an Incidence Greater than that in Patients Treated with Placebo Montelukast 10 mg/day (%) (n=1955) Placebo (%) (n=1180) Body As A Whole Pain, abdominal 2.9 2.5 Asthenia/fatigue 1.8 1.2 Fever 1.5 0.9 Trauma 1.0 0.8 Digestive System Disorders Dyspepsia 2.1 1.1 Pain, dental 1.7 1.0 Gastroenteritis, infectious 1.5 0.5 Nervous System/Psychiatric Headache 18.4 18.1 Dizziness 1.9 1.4 Respiratory System Disorders Influenza 4.2 3.9 Cough 2.7 2.4 Congestion, nasal 1.6 1.3 Skin/Skin Appendages Disorder Rash 1.6 1.2 Laboratory Adverse Experiences Number of patients tested (montelukast sodium and placebo, respectively): ALT and AST, 1935, 1170; pyuria, 1924, 1159. ALT increased 2.1 2.0 AST increased 1.6 1.2 Pyuria 1.0 0.9 The frequency of less common adverse events was comparable between montelukast sodium and placebo. The safety profile of montelukast sodium, when administered as a single dose for prevention of EIB in adult and adolescent patients 15 years of age and older, was consistent with the safety profile previously described for montelukast sodium. Cumulatively, 569 patients were treated with montelukast sodium for at least 6 months, 480 for one year, and 49 for two years in clinical trials. With prolonged treatment, the adverse experience profile did not significantly change. Adults and Adolescents 15 Years of Age and Older with Seasonal Allergic Rhinitis Montelukast sodium has been evaluated for safety in 2199 adult and adolescent patients 15 years of age and older in clinical trials. Montelukast sodium administered once daily in the morning or in the evening had a safety profile similar to that of placebo. In placebo-controlled clinical trials, the following event was reported with montelukast sodium with a frequency ≥ 1% and at an incidence greater than placebo: upper respiratory infection, 1.9% of patients receiving montelukast sodium vs. 1.5% of patients receiving placebo. In a 4-week, placebo-controlled clinical study, the safety profile was consistent with that observed in 2-week studies. The incidence of somnolence was similar to that of placebo in all studies. Adults and Adolescents 15 Years of Age and Older with Perennial Allergic Rhinitis Montelukast sodium has been evaluated for safety in 3357 adult and adolescent patients 15 years of age and older with perennial allergic rhinitis of whom 1632 received montelukast sodium in two, 6-week, clinical studies. Montelukast sodium administered once daily had a safety profile consistent with that observed in patients with seasonal allergic rhinitis and similar to that of placebo. In these two studies, the following events were reported with montelukast sodium with a frequency ≥ 1% and at an incidence greater than placebo: sinusitis, upper respiratory infection, sinus headache, cough, epistaxis, and increased ALT. The incidence of somnolence was similar to that of placebo. 6.2 Post-Marketing Experience The following adverse reactions have been identified during post-approval use of montelukast sodium. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. Blood and lymphatic system disorders: increased bleeding tendency, thrombocytopenia. Immune system disorders: hypersensitivity reactions including anaphylaxis, hepatic eosinophilic infiltration. Psychiatric disorders: agitation including aggressive behavior or hostility, anxiousness, depression, disorientation, disturbance in attention, dream abnormalities, hallucinations, insomnia, irritability, restlessness, somnambulism, suicidal thinking and behavior (including suicide), tic, and tremor [ see Warnings and Precautions (5.4 ) ]. Nervous system disorders: drowsiness, paraesthesia/hypoesthesia, seizures. Cardiac disorders: palpitations. Respiratory, thoracic and mediastinal disorders: epistaxis, pulmonary eosinophilia. Gastrointestinal disorders: diarrhea, dyspepsia, nausea, pancreatitis, vomiting. Hepatobiliary disorders: Cases of cholestatic hepatitis, hepatocellular liver-injury, and mixed-pattern liver injury have been reported in patients treated with montelukast sodium. Most of these occurred in combination with other confounding factors, such as use of other medications, or when montelukast sodium was administered to patients who had underlying potential for liver disease such as alcohol use or other forms of hepatitis. Skin and subcutaneous tissue disorders: angioedema, bruising, erythema multiforme, erythema nodosum,pruritus, Stevens-Johnson syndrome/toxic epidermal necrolysis, urticaria. Musculoskeletal and connective tissue disorders: arthralgia, myalgia including muscle cramps. Renal and urinary disorders: enuresis in children. General disorders and administration site conditions: edema. Patients with asthma on therapy with montelukast sodium may present with systemic eosinophilia, sometimes presenting with clinical features of vasculitis consistent with Churg-Strauss syndrome, a condition which is often treated with systemic corticosteroid therapy. These events have been sometimes associated with the reduction of oral corticosteroid therapy. Physicians should be alert to eosinophilia, vasculitic rash, worsening pulmonary symptoms, cardiac complications, and/or neuropathy presenting in their patients [ see Warnings and Precautions (5.5 ) ].
adverse reactions table
<table cellspacing="0" cellpadding="0" border="0" width="100%"><tbody><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"/><td align="center" styleCode="Rrule" valign="top">Montelukast 10 mg/day (%) (n=1955) </td><td align="center" styleCode="Rrule" valign="top">Placebo (%) (n=1180) </td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"><content styleCode="italics">Body As A Whole</content></td><td styleCode="Rrule" valign="top"/><td styleCode="Rrule" valign="top"/></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Pain, abdominal</td><td styleCode="Rrule" valign="top">2.9 </td><td styleCode="Rrule" valign="top">2.5</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Asthenia/fatigue</td><td styleCode="Rrule" valign="top">1.8</td><td styleCode="Rrule" valign="top">1.2</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Fever</td><td styleCode="Rrule" valign="top">1.5</td><td styleCode="Rrule" valign="top">0.9</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Trauma</td><td styleCode="Rrule" valign="top">1.0 </td><td styleCode="Rrule" valign="top">0.8</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"><content styleCode="italics">Digestive System Disorders</content></td><td styleCode="Rrule" valign="top"/><td styleCode="Rrule" valign="top"/></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Dyspepsia</td><td styleCode="Rrule" valign="top">2.1 </td><td styleCode="Rrule" valign="top">1.1</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Pain, dental</td><td styleCode="Rrule" valign="top">1.7</td><td styleCode="Rrule" valign="top">1.0</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Gastroenteritis, infectious</td><td styleCode="Rrule" valign="top">1.5 </td><td styleCode="Rrule" valign="top">0.5</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"><content styleCode="italics">Nervous System/Psychiatric</content></td><td styleCode="Rrule" valign="top"/><td styleCode="Rrule" valign="top"/></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Headache</td><td styleCode="Rrule" valign="top">18.4 </td><td styleCode="Rrule" valign="top">18.1</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Dizziness</td><td styleCode="Rrule" valign="top">1.9</td><td styleCode="Rrule" valign="top">1.4</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"><content styleCode="italics">Respiratory System Disorders</content></td><td styleCode="Rrule" valign="top"/><td styleCode="Rrule" valign="top"/></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Influenza</td><td styleCode="Rrule" valign="top">4.2 </td><td styleCode="Rrule" valign="top">3.9</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Cough</td><td styleCode="Rrule" valign="top">2.7</td><td styleCode="Rrule" valign="top">2.4</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Congestion, nasal</td><td styleCode="Rrule" valign="top">1.6 </td><td styleCode="Rrule" valign="top">1.3</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"><content styleCode="italics">Skin/Skin Appendages Disorder</content></td><td styleCode="Rrule" valign="top"/><td styleCode="Rrule" valign="top"/></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> Rash</td><td styleCode="Rrule" valign="top">1.6 </td><td styleCode="Rrule" valign="top">1.2</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"><content styleCode="italics">Laboratory Adverse Experiences <footnote ID="fn1560">Number of patients tested (montelukast sodium and placebo, respectively): ALT and AST, 1935, 1170; pyuria, 1924, 1159.</footnote></content></td><td styleCode="Rrule" valign="top"/><td styleCode="Rrule" valign="top"/></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> ALT increased</td><td styleCode="Rrule" valign="top">2.1 </td><td styleCode="Rrule" valign="top">2.0</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule" valign="top"> AST increased</td><td styleCode="Rrule" valign="top">1.6</td><td styleCode="Rrule" valign="top">1.2</td></tr><tr><td styleCode="Lrule Rrule" valign="top"> Pyuria</td><td styleCode="Rrule" valign="top">1.0</td><td styleCode="Rrule" valign="top">0.9</td></tr></tbody></table>
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.