Cefotaxime
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
- Cefotaxime
- Generic name
- CEFOTAXIME INJECTION
- Manufacturer
- SteriMax Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 8efe3bd0-c43a-2bd6-e053-2a95a90a92fa
- SPL ID
- 7a77a18a-3d8c-4bac-8d21-54a88db396f6
- Version
- 7
- Effective date
- 2026-06-15
- Source export date
- 2026-10-12
- 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/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:28:04
| Harmonized routes |
|---|
| INTRAMUSCULAR, INTRAVENOUS |
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 |
|---|---|---|---|
| brand name | Cefotaxime | openfda.brand_name | |
| generic name | CEFOTAXIME INJECTION | openfda.generic_name | |
| manufacturer name | SteriMax Inc. | openfda.manufacturer_name | |
| ndc | package | 21586-012-01 | openfda.package_ndc |
| ndc | package | 21586-011-02 | openfda.package_ndc |
| ndc | package | 21586-011-01 | openfda.package_ndc |
| ndc | package | 21586-012-02 | openfda.package_ndc |
| ndc | product | 21586-011 | openfda.product_ndc |
| ndc | product | 21586-012 | openfda.product_ndc |
| ndc11 | package | 21586001202 | derived:openfda.package_ndc |
| ndc11 | package | 21586001101 | derived:openfda.package_ndc |
| ndc11 | package | 21586001201 | derived:openfda.package_ndc |
| ndc11 | package | 21586001102 | derived:openfda.package_ndc |
| rxcui | 1656313 | openfda.rxcui | |
| rxcui | 1656318 | openfda.rxcui | |
| spl id | 7a77a18a-3d8c-4bac-8d21-54a88db396f6 | id | |
| spl set id | 8efe3bd0-c43a-2bd6-e053-2a95a90a92fa | set_id | |
| unii | 258J72S7TZ | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.