SUCRALFATE Oral Suspension

FDA Drug Profile — Sucralfate

SUCRALFATE Oral Suspension is listed in the FDA National Drug Code directory with 2 NDC codes, marketed under brand name including Sucralfate. Available dosage form: suspension.

Drug Details

Generic Name
SUCRALFATE Oral Suspension
Brand Names
Sucralfate
Application Number
ANDA211884
Sponsor
Major Pharmaceuticals
NDC Codes
2
Dosage Forms
SUSPENSION
Routes
ORAL
Active Ingredients
SUCRALFATE

Indications and Usage

INDICATIONS AND USAGE Sucralfate Oral Suspension is indicated in the short-term (up to 8weeks) treatment of active duodenal ulcer.

Warnings

WARNINGS Fatal complications, including pulmonary and cerebral emboli have occurred with inappropriate intravenous administration of Sucralfate Oral Suspension. Administer Sucralfate Oral Suspension only by the oral route. Do not administer intravenously.