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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
Zetia
Generic name / active ingredient
ezetimibe
Dosage-form class
Ezetimibe oral tablet: 10 mg (DailyMed page updated 25 Nov 2025; this dossier precisely displays NDC 78206-178-01, a 30-tablet bottle)
Route
Oral
Record reviewed
2026-08-21

Copy from the pack in hand

Source-linked reading points

  • Check ZETIA, ezetimibe, oral tablet, labelled strength per tablet and target market first. Appearing in the same discussion as atorvastatin, rosuvastatin or another lipid medicine does not permit self-adding on the same day, alternating or direct substitution from one pack to another.
  • Label information about use with other lipid medicines depends on the exact product, context, liver status, prior reactions and complete medicine list. A webpage does not turn “both are lipid medicines” into a combination conclusion for everyone.
  • The mg number is only an identity field for an exact tablet, not a personal algorithm for lipid results, risk or targets. Have a clinician or pharmacist review any start, stop, switch, splitting or combination question against the current label and real circumstances.
  • With muscle symptoms, marked fatigue, jaundice-like changes or another new concern, do not self-attribute it to one lipid medicine or stop multiple medicines at once; seek timely professional assessment with the complete medicine list.

Reviewed presentation examples — compare every field

  • 10 mg per tablet; 30-tablet bottleNDC 78206-178-01

EDITORIAL RECORD

Who prepared and checked this page

Byline
OriginDrug Content Editorial
Review role
Public primary-source verification
Last reviewed
2026-08-21
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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