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
- CVS Pharmacy, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 479a1437-a212-49d9-b272-758c0e5b7203
- SPL ID
- 1180f756-b6a5-4bc8-a16d-f54945aa6232
- Version
- 10
- Effective date
- 2025-04-22
- Source export date
- 2026-10-12
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:09:53
| 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 | CVS Pharmacy, Inc. | openfda.manufacturer_name | |
| ndc | package | 69842-087-80 | openfda.package_ndc |
| ndc | package | 69842-087-79 | openfda.package_ndc |
| ndc | package | 69842-087-53 | openfda.package_ndc |
| ndc | package | 69842-087-14 | openfda.package_ndc |
| ndc | package | 69842-087-21 | openfda.package_ndc |
| ndc | product | 69842-087 | openfda.product_ndc |
| ndc11 | package | 69842008780 | derived:openfda.package_ndc |
| ndc11 | package | 69842008753 | derived:openfda.package_ndc |
| ndc11 | package | 69842008714 | derived:openfda.package_ndc |
| ndc11 | package | 69842008779 | derived:openfda.package_ndc |
| ndc11 | package | 69842008721 | derived:openfda.package_ndc |
| rxcui | 310273 | openfda.rxcui | |
| spl id | 1180f756-b6a5-4bc8-a16d-f54945aa6232 | id | |
| spl set id | 479a1437-a212-49d9-b272-758c0e5b7203 | 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.