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Medicines · US (FDA)

FDA 2024

Other drugs for peptic ulcer and gastro-oesophageal reflux disease (GORD)

Sucralfate

Approved 23 Jul 2024OralSuspension

The FDA lists this product in 14 strengths and forms.

Official labelAsk Osler about it

On this page

Composition
Strengths and forms
Official product information

The table holds no label text for this product yet, only the facts beside it. The official product information has the full text.

Composition

Active ingredients: SUCRALFATE 1GM/10ML

Strengths and forms

The FDA lists each strength of a product separately; these pages share one label.

SUCRALFATE 1GM/10ML · SuspensionThis page
SUCRALFATE 1GM/10ML · SuspensionANDA216726-001 · Prescription
SUCRALFATE 1GM/10ML · SuspensionANDA211884-001 · Prescription
SUCRALFATE 1GM · TabletANDA215576-001 · Prescription
SUCRALFATE 1GM/10ML · SuspensionANDA212141-001 · Prescription
SUCRALFATE 1GM/10ML · SuspensionANDA213549-001 · Prescription
SUCRALFATE 1GM · TabletANDA215705-001 · Prescription
SUCRALFATE 1GM/10ML · SuspensionANDA216474-001 · Prescription
SUCRALFATE 1GM/10ML · SuspensionANDA217126-001 · Prescription
SUCRALFATE 1GM/10ML · SuspensionANDA211780-001 · Prescription
SUCRALFATE 1GM · TabletANDA074415-001 · Prescription
SUCRALFATE 1GM · TabletANDA070848-001 · Prescription

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

SUCRALFATE 1GM/10ML · SuspensionANDA209356-001 · Prescription

SUCRALFATE 1GM/10ML · SuspensionANDA212913-001 · Prescription

Official product information

Drugs@FDA lists the approved labels, letters and reviews for application ANDA212769.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Brand name: Sucralfate
Drug class: Other drugs for peptic ulcer and gastro-oesophageal reflux disease (GORD)
Route: Oral
Dosage form: Suspension
Applicant: Hikma
Status: Discontinued
FDA approval: 23 Jul 2024
Application: ANDA212769-001
RxCUI: 10156