warnings
Warnings Allergy alert: Do not use if you are allergic to famotidine or other acid reducers
Famotidine
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
- Famotidine
- Generic name
- FAMOTIDINE
- Manufacturer
- Aurohealth LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5b161f25-c578-4ff4-a931-ff3a1e681c50
- SPL ID
- 2c043b30-86e8-4c8a-b247-d9b6e72a3dbc
- Version
- 10
- Effective date
- 2026-09-04
- Source export date
- 2026-10-27
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:45:48
| 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 | 206531 | derived:openfda.application_number |
| application number | ANDA206531 | openfda.application_number | |
| brand name | Famotidine | openfda.brand_name | |
| generic name | FAMOTIDINE | openfda.generic_name | |
| manufacturer name | Aurohealth LLC | openfda.manufacturer_name | |
| ndc | package | 58602-829-34 | openfda.package_ndc |
| ndc | package | 58602-829-21 | openfda.package_ndc |
| ndc | package | 58602-829-50 | openfda.package_ndc |
| ndc | product | 58602-829 | openfda.product_ndc |
| ndc11 | package | 58602082921 | derived:openfda.package_ndc |
| ndc11 | package | 58602082934 | derived:openfda.package_ndc |
| ndc11 | package | 58602082950 | derived:openfda.package_ndc |
| rxcui | 310273 | openfda.rxcui | |
| spl id | 2c043b30-86e8-4c8a-b247-d9b6e72a3dbc | id | |
| spl set id | 5b161f25-c578-4ff4-a931-ff3a1e681c50 | set_id | |
| unii | 5QZO15J2Z8 | 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.