warnings
Warnings Allergy alert: Do not use if you are allergic to omeprazole Omeprazole may cause severe skin reactions. Symptoms may include: skin reddening blisters rash if an allergic reaction occurs, stop use and seek medical help right away.
Omeprazole
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Omeprazole
- Generic name
- OMEPRAZOLE
- Manufacturer
- WALMART INC. (see also Equate)
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d3c1ba08-680d-4e39-875c-1f1d42ae787c
- SPL ID
- 1fabf3d4-e22f-474e-8812-679544cc48aa
- Version
- 4
- Effective date
- 2026-07-13
- Source export date
- 2026-10-27
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:26:30
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 206582 | derived:openfda.application_number |
| application number | ANDA206582 | openfda.application_number | |
| brand name | Omeprazole | openfda.brand_name | |
| generic name | OMEPRAZOLE | openfda.generic_name | |
| manufacturer name | WALMART INC. (see also Equate) | openfda.manufacturer_name | |
| ndc | package | 79903-377-42 | openfda.package_ndc |
| ndc | package | 79903-377-14 | openfda.package_ndc |
| ndc | product | 79903-377 | openfda.product_ndc |
| ndc11 | package | 79903037714 | derived:openfda.package_ndc |
| ndc11 | package | 79903037742 | derived:openfda.package_ndc |
| rxcui | 402014 | openfda.rxcui | |
| spl id | 1fabf3d4-e22f-474e-8812-679544cc48aa | id | |
| spl set id | d3c1ba08-680d-4e39-875c-1f1d42ae787c | set_id | |
| unii | 426QFE7XLK | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.