warnings
WARNINGS Allergy alert: Do not use if you are allergic to ranitidine or other acid reducers
Ranitidine
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
- Ranitidine
- Generic name
- RANITIDINE
- Manufacturer
- Granules India Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- aab81d9f-397d-49fb-8083-77a1872cc71f
- SPL ID
- 44f2b222-ae43-eef4-e063-6394a90ab2b6
- Version
- 11
- Effective date
- 2025-12-02
- Source export date
- 2026-09-28
- 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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:49
| 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 | 210243 | derived:openfda.application_number |
| application number | ANDA210243 | openfda.application_number | |
| brand name | Ranitidine cool mint | openfda.brand_name | |
| brand name | Ranitidine | openfda.brand_name | |
| generic name | RANITIDINE | openfda.generic_name | |
| manufacturer name | Granules India Ltd | openfda.manufacturer_name | |
| ndc | package | 62207-773-58 | openfda.package_ndc |
| ndc | package | 62207-774-36 | openfda.package_ndc |
| ndc | package | 62207-773-41 | openfda.package_ndc |
| ndc | package | 62207-773-32 | openfda.package_ndc |
| ndc | package | 62207-774-58 | openfda.package_ndc |
| ndc | package | 62207-774-47 | openfda.package_ndc |
| ndc | package | 62207-773-47 | openfda.package_ndc |
| ndc | package | 62207-774-41 | openfda.package_ndc |
| ndc | package | 62207-773-36 | openfda.package_ndc |
| ndc | product | 62207-773 | openfda.product_ndc |
| ndc | product | 62207-774 | openfda.product_ndc |
| ndc11 | package | 62207077436 | derived:openfda.package_ndc |
| ndc11 | package | 62207077332 | derived:openfda.package_ndc |
| ndc11 | package | 62207077341 | derived:openfda.package_ndc |
| ndc11 | package | 62207077458 | derived:openfda.package_ndc |
| ndc11 | package | 62207077336 | derived:openfda.package_ndc |
| ndc11 | package | 62207077447 | derived:openfda.package_ndc |
| ndc11 | package | 62207077347 | derived:openfda.package_ndc |
| ndc11 | package | 62207077441 | derived:openfda.package_ndc |
| ndc11 | package | 62207077358 | derived:openfda.package_ndc |
| rxcui | 198191 | openfda.rxcui | |
| spl id | 44f2b222-ae43-eef4-e063-6394a90ab2b6 | id | |
| spl set id | aab81d9f-397d-49fb-8083-77a1872cc71f | set_id | |
| unii | BK76465IHM | 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.