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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
Iressa
Generic name / active ingredient
gefitinib
Dosage-form class
Dosage form and presentation as documented in the linked primary label
Route
Oral
Record reviewed
2026-08-23

Copy from the pack in hand

Source-linked reading points

  • This public label lists 250 mg film-coated oral tablets; round, brown, biconvex tablets debossed “IRESSA 250” are identity clues in this U.S. label. Check mg, appearance, pack count and brand together. A difference in any one of them does not establish the same product, authenticity or packaging in another market.
  • The label gives a specific water-dispersion procedure for this exact tablet when solid dosage forms cannot be swallowed. It is not general permission to split, crush, store, or mix tablets with food or another liquid; handling of an actual pack needs confirmation against the current target-market label by the oncology team or pharmacist.
  • The label flags enzyme inducers/inhibitors that affect gefitinib exposure, medicines affecting gastric acidity and warfarin-related bleeding monitoring. Stomach medicines, anti-infectives, herbs, anticoagulants and every prescription/OTC product should be reviewed with the actual packages by the oncology team or pharmacist; a webpage cannot decide individual co-use, spacing or adjustment.
  • With new or worsening breathing difficulty, cough or fever, persistent or severe diarrhoea, jaundice-like changes, severe rash/blistering, eye pain or vision change, contact the treatment team promptly or use local urgent medical support. Do not self-pause, restart or change to another EGFR medicine from a webpage, one test result or another patient's experience.

Reviewed presentation examples — compare every field

  • 250 mg per tablet, 30-tablet bottleNDC 0310-0482-30

EDITORIAL RECORD

Who prepared and checked this page

Byline
OriginDrug Content Editorial
Review role
Public primary-source verification
Last reviewed
2026-08-23
Source record
3 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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