omeprazole 2 MG/ML / NaHCO3 84 MG/ML Oral Suspension

RxCUI
2625144
RxNorm name
omeprazole 2 MG/ML / NaHCO3 84 MG/ML Oral Suspension
Display name
omeprazole 2 MG/ML / NaHCO3 84 MG/ML Oral Suspension
Full name
omeprazole 2 MG/ML / NaHCO3 84 MG/ML Oral Suspension
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:02

RxNav Current And Historical NDCs#

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UNII Substances#

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openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
KonvomepOMEPRAZOLE AND SODIUM BICARBONATEAzurity Pharmaceuticals, Inc.688ed6f1-d78a-4006-a682-57021cb38a3e2025-12-16Warnings, Adverse reactionsExact identifier
rxcui: 2625144

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
688ed6f1-d78a-4006-a682-57021cb38a3eomeprazole 2 MG/ML / NaHCO3 84 MG/ML Oral SuspensionSY6These highlights do not include all the information needed to use KONVOMEP safely and effectively. See full prescribing information for KONVOMEP . KONVOMEP ® (omeprazole and sodium bicarbonate for oral suspension) Initial U.S. Approval: 200420251216
688ed6f1-d78a-4006-a682-57021cb38a3eomeprazole 2 MG/ML / sodium bicarbonate 84 MG/ML Oral SuspensionSCD6These highlights do not include all the information needed to use KONVOMEP safely and effectively. See full prescribing information for KONVOMEP . KONVOMEP ® (omeprazole and sodium bicarbonate for oral suspension) Initial U.S. Approval: 200420251216
688ed6f1-d78a-4006-a682-57021cb38a3eomeprazole 2 MG/mL / sodium bicarbonate 84 MG/mL Oral SuspensionPSN6These highlights do not include all the information needed to use KONVOMEP safely and effectively. See full prescribing information for KONVOMEP . KONVOMEP ® (omeprazole and sodium bicarbonate for oral suspension) Initial U.S. Approval: 200420251216