PACK IN HAND · ONE-PAGE CHECK
Medicine pack check sheet
Print this sheet or fill it in before speaking with a pharmacist or clinician. Copy only what is printed on the pack in hand. The published fields below are starting points from this record, not proof that your pack is the same product.
Published record starting point
- Record display name
- Singulair
- Generic name / active ingredient
- montelukast
- Dosage-form class
- Film-coated tablets, chewable tablets and oral granules (as documented in this dossier)
- Route
- Oral
- Record reviewed
- 2026-08-22
Copy from the pack in hand
Source-linked reading points
- Check SINGULAIR, montelukast sodium, the exact form, stated strength per unit and target market together. A shared non-proprietary name does not make film-coated tablets, chewables and granules self-convertible or substitutable by tablet count, sachet count or experience.
- The label includes a neuropsychiatric-events warning. With a new or concerning change in mood, behaviour, sleep or thinking, promptly contact a professional through local medical channels; do not self-stop, restart, increase or change to another medicine from a webpage.
- The label also says this product is not for reversal of acute bronchospasm. Sudden or worsening breathing difficulty should not be managed by self-escalation, waiting for a webpage or borrowing another person's medicine; use local emergency and care-team guidance.
- Package images, a name and “allergy/asthma” wording only help locate a label. They cannot authenticate a product, establish current approval or prove interchangeability with another allergy, inhaled or rescue product. Ask a pharmacist to review the complete medicine list with every addition, stop or change.
Reviewed presentation examples — compare every field
- Montelukast sodium 4 mg oral granules; 30-packet cartonNDC 78206-171-01
- Montelukast sodium 4 mg chewable tablet; 30-tablet bottleNDC 78206-170-01
- Montelukast sodium 5 mg chewable tablet; 30-tablet bottleNDC 78206-173-01
- Montelukast sodium 10 mg film-coated tablet; 30-tablet bottleNDC 78206-172-01