FDA.reportPublic FDA data

NDC 21586-011-01 - Cefotaxime

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
21586-011
Requested NDC
21586-011-01
Package NDCs from labels
21586-011-01, 21586-011-02
Manufacturer
SteriMax Inc.
Effective date
2026-06-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
cefotaxime injection - SteriMax Inc.SteriMax Inc.2026-06-15HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21586-011-01Cefotaxime1 in 1 VIALPOWDER, FOR SOLUTION16
21586-011-02Cefotaxime10 in 1 PACKAGEPOWDER, FOR SOLUTION106

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21586-011CEFOTAXIME (CEFOTAXIME INJECTION) POWDER, FOR SOLUTION [STERIMAX INC.]6Current NDC, Legacy NDC, 2 package rows20241215_8efe3bd0-c43a-2bd6-e053-2a95a90a92fa.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
21586-011-01EA - Each21586-01168a635ef-a8aa-4888-bbe0-f582204d6fdc12022-11-07
21586-011-02EA - Each21586-011605844a2-e1fc-49ab-b24f-8e5308d55fd412022-11-07

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 ยท 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CefotaximeCEFOTAXIME INJECTIONSteriMax Inc.8efe3bd0-c43a-2bd6-e053-2a95a90a92fa2026-06-15Exact identifier
ndc (package): 21586-012-01
ndc (package): 21586-011-02
ndc (package): 21586-011-01
ndc (package): 21586-012-02
ndc (product): 21586-011
ndc (product): 21586-012
ndc11 (package): 21586001101
rxcui: 1656313
rxcui: 1656318
spl id: 7a77a18a-3d8c-4bac-8d21-54a88db396f6
spl set id: 8efe3bd0-c43a-2bd6-e053-2a95a90a92fa
unii: 258J72S7TZ
CefotaximeCEFOTAXIMEHikma Pharmaceuticals USA Inc.ed23b6bc-32c7-4c50-a53d-313ae78e56232024-04-11Warnings, Adverse reactionsExact identifier
rxcui: 1656313
rxcui: 1656318
unii: 258J72S7TZ
CefotaximeCEFOTAXIMEHikma Pharmaceuticals USA Inc.ef1a6dc6-bc3d-4f09-8f92-7ff328f565612024-04-11Warnings, Adverse reactionsExact identifier
unii: 258J72S7TZ

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.