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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
Lasix
Generic name / active ingredient
furosemide
Dosage-form class
Oral tablets(as listed in the 2018 FDA label archive and 2025-10 DailyMed public label)
Route
Oral
Record reviewed
2026-08-17

Copy from the pack in hand

Source-linked reading points

  • The public label lists 20, 40 and 80 mg oral tablets. Each number first describes the stated strength of one tablet; remaining tablets, weight change, ankle swelling or one episode of urine output do not allow a reader to assemble different strengths into a new personal tablet count.
  • The label identifies changes in fluid and electrolytes, hypotension, kidney function and medicine-related issues as matters for professional review. With older age, multiple medicines, changed intake, recent vomiting or diarrhoea, or around testing and procedures, use the complete medicine list and actual package for clinician or pharmacist review rather than self-adjusting from pack colour or the word “diuretic.”
  • A name or overlapping purpose with another “blood-pressure medicine,” “diuretic” or supplement does not automatically establish that products can be combined, alternated or substituted. Duplication, interactions and a need for laboratory monitoring must be confirmed by the prescribing team using the exact products and individual information.
  • Package appearance, a 40 mg marking or bottle count only help locate a source. They cannot authenticate a medicine, establish current market approval or determine individual use. With fainting, marked weakness, altered awareness, severe illness or uncertainty about use, use local urgent-care and professional contact pathways.

Reviewed presentation examples — compare every field

  • Furosemide 20 mg per tablet; 100-tablet bottleNDC 30698-067-01
  • Furosemide 40 mg per tablet; 100-tablet bottleNDC 30698-060-01
  • Furosemide 80 mg per tablet; 50-tablet bottleNDC 30698-066-05

EDITORIAL RECORD

Who prepared and checked this page

Byline
OriginDrug Content Editorial
Review role
Public primary-source verification
Last reviewed
2026-08-17
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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