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
- Amoxil
- Generic name / active ingredient
- amoxicillin
- Dosage-form class
- Dosage form and presentation as documented in the linked primary label
- Route
- Oral
- Record reviewed
- 2026-09-02
Copy from the pack in hand
Source-linked reading points
- ‘500 mg per tablet’ and ‘400 mg per 5 mL’ are label units for different forms. Pack numbers cannot answer how many tablets or millilitres an individual should take; diagnosis, age or weight, kidney function, exact product, prescription and target-market label are all required.
- The score on the 875 mg tablet is an appearance feature of that labelled product, not permission to halve, reduce or substitute another strength. Splitting, administration or changing to suspension requires the exact current label and pharmacist review against the prescription.
- The 200 mg and 400 mg chewables contain aspartame, and the FDA label lists phenylalanine information. This does not mean they are unsuitable for everyone, but phenylketonuria and related concerns require review of the exact product with a professional.
- With a serious penicillin or cephalosporin allergy history, breathing trouble or widespread rash after use, severe or persistent diarrhoea, or co-use of anticoagulants, allopurinol or other medicines, contact a local clinician or pharmacist promptly. Severe breathing difficulty, face/lip/tongue swelling or fainting requires emergency care.
Reviewed presentation examples — compare every field
- 500 mg; 100-tablet bottle, 500-tablet bottle or 20-tablet packNDC 81964-024-01 / 81964-024-05 / 81964-024-14
- 875 mg; 100-tablet bottle or 20-tablet packNDC 81964-019-01 / 81964-019-14
- 200 mg/5 mL; 50, 75 or 100 mL bottle after reconstitutionNDC 81964-023-50 / 81964-023-51 / 81964-023-52
- 400 mg/5 mL; 50, 75 or 100 mL bottle after reconstitutionNDC 81964-007-50 / 81964-007-51 / 81964-007-52
- 125 mg; 60- or 100-tablet bottleNDC 81964-026-60 / 81964-026-01
- 200 mg; 20-tablet unit-dose packNDC 81964-028-14
- 250 mg; 30- or 100-tablet bottleNDC 81964-027-30 / 81964-027-01
- 400 mg; 20-tablet unit-dose pack or 100-tablet bottleNDC 81964-029-14 / 81964-029-01