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Sucralfate 1 g

INDICATIONS AND USAGE Sucralfate tablets, USP are indicated in: Short-term treatment (up to 8 weeks) of active duodenal ulcer. While healing with sucralfate may occur during the first week or two, treatment should be continued for 4 to 8 weeks unless healing has been demonstrated by x-ray or endoscopic examination. Maintenance therapy for duodenal ulcer patients at reduced dosage after healing of acute ulcers.

Teva Pharmaceuticals USA Inc

FDA Reported Adverse Reactions
[1] drug ineffective    [2] fatigue    [3] nausea    [4] pain    [5] diarrhoea    [6] headache    [7] off label use    [8] dyspnoea    [9] vomiting    [10] rash   

7 years ago OVAL WHITE Teva 22 10 Sucralfate 1 g

OVAL WHITE Teva 22 10

7 years ago OVAL WHITE Teva 22 10 Sucralfate 1 g

Teva 22 10 OVAL WHITE

HOW SUPPLIED

SUCRALFATE tablets, USP are available as white, capsule-shaped, biconvex, scored tablets, debossed “TEVA” on one side, and “22” and “10” on the scored side, containing 1 gram of

SUCRALFATE USP, packaged in bottles of 90 (NDC 0093-2210-98), 100 (NDC 0093-2210-01) and 500 (NDC 0093-2210-05) tablets. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required). KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN. Manufactured In Croatia By: PLIVA HRVATSKA d.o.o. Zagreb, Croatia Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454 Rev. L 9/2015


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