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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

EDITORIAL RECORD

Who prepared and checked this page

Byline
OriginDrug Content Editorial
Review role
Public primary-source verification
Last reviewed
2026-08-22
Source record
2 clickable primary-source entry points are listed with this dossier.

The review role checks source traceability, stated market, document version and product-identity fields. It is not a claim of clinical licensure, prescribing authority or individual pharmacy service. Read the editorial policy.

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