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These highlights do not include all the information needed to use ZEGERID safely and effectively. See full prescribing information for ZEGERID.ZEGERID® (omeprazole and sodium bicarbonate) for oral suspensionZEGERID® (omeprazole and sodium bicarbonate) capsules, for oral useInitial U.S. Approval: 2004
Medication labelWhy this: Advisory · dailymed-prescription
ZEGERID for oral suspension and ZEGERID capsules are indicated in adults for the: •short-term treatment of active duodenal ulcer. Most patients heal within four weeks. Some patients may require an additional four weeks of therapy. •short-term treatment (4 to 8 weeks) of active benign gastric ulcer. •treatment of heartburn and other symptoms associated with GERD for up to 4 weeks. •short-term treatment (4 to 8 weeks) of EE due to acid-mediated GERD which has been diagnosed by endoscopy in adults. oThe efficacy of ZEGERID used for longer than 8 weeks in patients with EE has not been established. If a patient does not respond to 8 weeks of treatment, an additional 4 weeks of treatment may be given. If there is recurrence of EE or GERD symptoms (e.g., heartburn), additional 4 to 8-week courses of ZEGERID may be considered. •maintenance of healing of EE due to acid-mediated GERD. Controlled studies do not extend beyond 12 months. ZEGERID for oral suspension is indicated in adults for the: •reduction of risk of upper GI bleeding in critically ill adult patients.
- generic_name
- omeprazole and sodium bicarbonate
- product_names
- omeprazole and sodium bicarbonate
- ndc
- 68012-102, 68012-104, 68012-052, 68012-054, 68012-052-30, 68012-054-30, 68012-054-03, 68012-102-30, 68012-104-30, 68012-104-05
- group
- drugs
- license
- us-gov-pd
- attribution
- Courtesy of the National Library of Medicine
- reviewed
- 2026-09-18
- language
- en