Carafate 1g 120 Tablets

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Carafate 1g 120 Tablets. Treatment of gastric and duodenal ulcer under medical supervision.

The estimated expiry for this product is JUN2027. It was last checked and updated on 20FEB2026. This is an indicative expiry based upon the last stock check and may vary at the time of supply. Images and information supplied on the website are for representation purposes only. Actual product may differ from images shown. Please contact us to verify if you are looking for a specific packaging or formulation prior to making an order. We will always endeavour to supply the latest product packaging and formulations from the manufacturer with the longest expiry possible.

Carafate 1g 120 Tablets

Key facts
  • Product type: Medicine — Registered (AUST R)
  • Used for: a Schedule 4 oral sucralfate preparation used in the treatment of active gastric and duodenal ulcer in adults under medical direction
  • ARTG listing: AUST R 14930
  • Australian sponsor: Viatris Pty Ltd
  • Schedule: S4 (Prescription Only)
  • Pack size: 120 tablets per bottle
  • Last reviewed: 29 May 2026
Carafate 1g 120 Tablets is a Schedule 4 oral sucralfate preparation used in the treatment of active gastric and duodenal ulcer in adults under medical direction. Refer to the carton and to your pharmacist or doctor for advice on whether this product is right for you.

Product specification

ARTG ID14930
Listing / registration numberAUST R 14930
Product typeMedicine — Registered (AUST R)
Australian sponsorViatris Pty Ltd
Dosage formUncoated oral tablet
Route of administrationOral
Pack size120 tablets per bottle
Active ingredientsSucralfate 1 g per uncoated tablet
ScheduleS4 (Prescription Only)
StorageStore below 30°C in a dry place, away from direct sunlight. Keep out of reach of children.

About this product

Carafate 1g 120 Tablets is a Schedule 4 oral sucralfate preparation used in the treatment of active gastric and duodenal ulcer in adults under medical direction. Supplied in Australia by Viatris Pty Ltd. Use it in accordance with the carton instructions and your healthcare professional's advice.

About the active

Sucralfate 1 g

Sucralfate is a basic aluminium salt of sulphated sucrose. In the acidic environment of the stomach it forms a viscous, adherent paste that binds preferentially to areas of ulcerated mucosa, producing a protective barrier against acid, pepsin and bile.

Unlike acid-suppressing medicines, sucralfate has minimal systemic absorption — its action is essentially local within the gastrointestinal tract.

Indicated for the treatment of gastric and duodenal ulcer under medical supervision, and for the treatment and prophylaxis of stress-induced gastric mucosal damage. The typical course is 4 to 8 weeks; treatment beyond this should be reviewed by the prescribing doctor.

Safety: Schedule 4 (Prescription Only). Discuss with the prescriber if you have kidney impairment (sucralfate contains aluminium), are pregnant or breastfeeding, or take other oral medicines — sucralfate may reduce the absorption of several medications (including certain antibiotics, thyroxine, digoxin, phenytoin). Separate doses of sucralfate from other oral medicines by at least 2 hours where possible. Constipation is a common, generally mild side effect.

Indications

The following indications are recorded on this product's ARTG entry:

  • Treatment of gastric and duodenal ulcer under medical supervision
  • Treatment and prophylaxis of stress-induced gastric mucosal damage

Directions for use

Adults: 1 g (one tablet) four times daily on an empty stomach, typically one hour before meals and at bedtime, or as directed by the prescribing doctor.

Warnings and important information

  • Always read the label and follow the directions for use.
  • If symptoms persist, talk to your healthcare professional.
  • Discuss with your pharmacist or doctor before use during pregnancy or breastfeeding.
  • Keep out of reach of children.
  • Do not use after the expiry date printed on the pack.
  • Stop use and seek advice if any unexpected reaction occurs.

Storage

Store below 30°C in a dry place, away from direct sunlight. Keep the original packaging closed. Keep out of reach of children. Do not use after the expiry date printed on the pack.

Frequently asked questions

What is Carafate used for?

Carafate is a Schedule 4 oral sucralfate preparation used in the treatment of active gastric and duodenal ulcer in adults under medical direction. It is supplied in Australia by Viatris Pty Ltd. Refer to your pharmacist or doctor for advice on whether the product is suitable for you.

How does Carafate work?

The active in Carafate is described in detail under 'About the active' above. The mechanism of action is summarised there in plain English.

What are the active ingredients in Carafate?

Carafate contains Sucralfate 1 g per uncoated tablet. The full active panel is shown in the Product Specification table above.

How do I take Carafate?

Adults: 1 g (one tablet) four times daily on an empty stomach, typically one hour before meals and at bedtime, or as directed by the prescribing doctor.

What are the possible side effects?

Refer to the Consumer Medicine Information leaflet supplied with the pack and to your pharmacist for the full side-effect profile. Stop use and seek advice if any unexpected reaction occurs.

Can I take this with my other prescription medicines?

Several common medicines interact with Carafate. Bring the pack to your pharmacist and ask them to check it against your current medicines list before starting.

Is this suitable during pregnancy or breastfeeding?

Use during pregnancy or breastfeeding is not recommended without professional advice. Refer to the carton and confirm with your pharmacist or doctor.

What should I do if I miss a dose?

If you miss a dose of Carafate, take it as soon as you remember unless it is nearly time for your next dose — in that case, skip the missed dose and continue with your usual schedule. If you have taken more than the directed amount, call the Poisons Information Centre on 13 11 26 (Australia) for advice.

Is this medicine TGA approved?

Yes. Carafate is a Registered (AUST R) medicine on the Australian Register of Therapeutic Goods, individually evaluated by the TGA for safety, quality and efficacy. The AUST R number is 14930 — you can verify the entry at tga.gov.au/resources/artg/14930.

Where is it manufactured?

Carafate is supplied in Australia by Viatris Pty Ltd.

When to seek further advice

This information is general in nature and is not a substitute for professional medical advice. If you have questions about whether Carafate is right for you, speak with your pharmacist or doctor. For 24-hour health advice in Australia, call Healthdirect on 1800 022 222. For poisoning enquiries, call the Poisons Information Centre on 13 11 26.

Sources

  • Australian Register of Therapeutic Goods (ARTG) — entry for this product. tga.gov.au/resources/artg
  • Therapeutic Goods Administration — Permissible Indications Determination and Therapeutic Goods (Therapeutic Goods Advertising Code) Instrument 2021. tga.gov.au
  • Healthdirect Australia — general consumer health information. healthdirect.gov.au
  • Manufacturer carton and Consumer Medicine Information (where supplied).


ALWAYS READ THE LABEL ON THE PRODUCT AND FOLLOW THE DIRECTIONS FOR USE UNLESS DIRECTED BY YOUR HEALTHCARE PROFESSIONAL.

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(Product SKU 497096)

SKU 497096
Barcode # 9323610014641
Shipping Cubic 0.000420000m3
Assembled Length 0.123m
Assembled Height 0.054m
Assembled Width 0.054m

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