FDA.reportPublic FDA data

NDC 0409-7338-21 - Ceftriaxone Sodium

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
0409-7338
Requested NDC
0409-7338-21
Package NDCs from labels
0409-7338-11, 0409-7338-01, 0409-7338-21, 0409-7338-20
Manufacturer
Hospira, Inc
Effective date
2026-01-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ceftriaxone Sodium - Hospira, IncHospira, Inc2026-01-19HUMAN PRESCRIPTION DRUG LABEL
Ceftriaxone Sodium - Hospira, IncHospira, Inc2026-01-19HUMAN PRESCRIPTION DRUG LABEL
Ceftriaxone Sodium - A-S Medication SolutionsA-S Medication Solutions2024-03-27HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0409-7338-01Ceftriaxone Sodium10 in 1 CARTONINJECTION, POWDER, FOR SOLUTION1021
0409-7338-11Ceftriaxone Sodium1 in 1 VIAL, SINGLE-USEINJECTION, POWDER, FOR SOLUTION121
0409-7338-20Ceftriaxone Sodium10 in 1 CARTONINJECTION, POWDER, FOR SOLUTION105
0409-7338-21Ceftriaxone Sodium1 in 1 VIAL, SINGLE-USEINJECTION, POWDER, FOR SOLUTION15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0409-7338CEFTRIAXONE SODIUM INJECTION, POWDER, FOR SOLUTION [HOSPIRA, INC]20Current NDC, Legacy NDC, 2 package rows20240113_03283208-8616-4117-9d2b-aa8046017a4f.zip
0409-7338CEFTRIAXONE SODIUM INJECTION, POWDER, FOR SOLUTION [HOSPIRA, INC]4Current NDC, Legacy NDC, 2 package rows20240113_19141ccd-e66c-49a2-a794-0616028495a7.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0409-7338-01EA - Each0409-733861ca6f98-68a6-41ea-a6d0-682fae528a9512012-07-24
0409-7338-11EA - Each0409-7338f1b4dc94-8e28-4672-8bf1-9be3b248797312018-08-13
0409-7338-20EA - Each0409-73380a901cde-513e-4112-95a0-e66da93d0c2a12018-04-19

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CEFTRIAXONE SODIUMACTIVE INGREDIENT023Z5BR09KCEFTRIAXONE SODIUM INJECTION, POWDER, FOR SOLUTION [HOSPIRA, INC]16
CEFTRIAXONEACTIVE MOIETY75J73V1629CEFTRIAXONE SODIUM INJECTION, POWDER, FOR SOLUTION [HOSPIRA, INC]16

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 2 · 35 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ceftriaxone SodiumCEFTRIAXONE SODIUMSportpharm LLCddbc3bf6-5bab-4851-ae5a-ef263cd8f2552026-07-23Warnings, Adverse reactionsExact identifier
application number: ANDA065169
rxcui: 1665005
rxcui: 309092
rxcui: 1665021
unii: 023Z5BR09K
CeftriaxoneCEFTRIAXONEWG Critical Care, LLC86ec0a92-a552-4a6d-9125-a54f95e433922026-06-18Warnings, Adverse reactionsExact identifier
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMSportpharm LLC85ce4f8b-77e0-48bf-9f57-93f1478befa22026-04-24Warnings, Adverse reactionsExact identifier
rxcui: 1665021
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMSportpharm LLC9a937e47-8c36-4656-83e1-b3c18ed9bac32026-04-24Warnings, Adverse reactionsExact identifier
rxcui: 1665005
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMREMEDYREPACK INC.9c801096-ca61-4b29-a1e1-5f7e7813b1912026-02-06Warnings, Adverse reactionsExact identifier
application number: ANDA065169
rxcui: 1665021
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMQilu Pharmaceutical Co., Ltd.4cdf0743-c62b-4969-b9c9-4c6400644f6c2026-02-04Warnings, Adverse reactionsExact identifier
rxcui: 1665046
rxcui: 1665005
rxcui: 309092
rxcui: 1665021
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMHospira, Inc128bb292-d174-4769-b3e6-9f16617f31e32026-01-22Warnings, Adverse reactionsExact identifier
rxcui: 1665046
rxcui: 1665021
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMHospira, Inc19141ccd-e66c-49a2-a794-0616028495a72026-01-19Warnings, Adverse reactionsExact identifier
application number: ANDA065169
ndc (package): 0409-7338-20
ndc (package): 0409-7338-21
ndc (package): 0409-7332-21
ndc (package): 0409-7335-21
ndc (package): 0409-7332-20
ndc (package): 0409-7337-20
ndc (package): 0409-7335-20
ndc (package): 0409-7337-21
ndc (product): 0409-7338
ndc (product): 0409-7335
ndc (product): 0409-7332
ndc (product): 0409-7337
ndc11 (package): 00409733821
rxcui: 1665046
rxcui: 1665005
rxcui: 309092
rxcui: 1665021
spl id: c4d53472-41a6-428e-8935-f2c611729457
spl set id: 19141ccd-e66c-49a2-a794-0616028495a7
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMHospira, Inc03283208-8616-4117-9d2b-aa8046017a4f2026-01-19Warnings, Adverse reactionsExact identifier
application number: ANDA065169
ndc (package): 0409-7338-11
ndc (package): 0409-7337-01
ndc (package): 0409-7337-11
ndc (package): 0409-7335-03
ndc (package): 0409-7332-01
ndc (package): 0409-7332-11
ndc (package): 0409-7338-01
ndc (package): 0409-7335-13
ndc (product): 0409-7338
ndc (product): 0409-7335
ndc (product): 0409-7332
ndc (product): 0409-7337
rxcui: 1665046
rxcui: 1665005
rxcui: 309092
rxcui: 1665021
spl id: cc7743b1-4e7b-446a-9ec1-cc234a8bbccf
spl set id: 03283208-8616-4117-9d2b-aa8046017a4f
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMHospira, Inc365fc265-8e6c-432f-9fda-911f5f7fb4512026-01-16Warnings, Adverse reactionsExact identifier
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMHospira, Inc36c07ebf-b091-483e-b2c4-f0fc0c2b41862026-01-16Warnings, Adverse reactionsExact identifier
unii: 023Z5BR09K
CeftriaxoneCEFTRIAXONEWG Critical Care, LLC7bed9b33-29e3-4f04-9766-43a21c7ad47a2026-01-07Warnings, Adverse reactionsExact identifier
rxcui: 1665046
rxcui: 1665021
unii: 023Z5BR09K
CeftriaxoneCEFTRIAXONEWG Critical Care, LLCbefd73ff-cb3b-4543-8a8e-bdb9b7fc1ff02025-04-07Warnings, Adverse reactionsExact identifier
rxcui: 1665046
rxcui: 1665005
rxcui: 1665021
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMSandoz Inc53df951b-2eee-44b1-bae2-df7ed85bc0ed2025-02-28Warnings, Adverse reactionsExact identifier
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMSandoz Incde028434-46cf-44f6-8ac6-889c7c6943b32025-02-27Warnings, Adverse reactionsExact identifier
application number: ANDA065169
rxcui: 1665046
rxcui: 1665005
rxcui: 309092
rxcui: 1665021
unii: 023Z5BR09K
CeftriaxoneCEFTRIAXONE SODIUMBaxter Healthcare Company4c5c2d3f-5038-41a1-a2fe-4dcd048dbac12024-10-07Warnings, Adverse reactionsExact identifier
rxcui: 1665046
rxcui: 1665021
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMA-S Medication Solutions53415af6-4072-4339-83e2-d870ae02a0e22024-08-20Warnings, Adverse reactionsExact identifier
rxcui: 1665005
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMA-S Medication Solutionsb642877e-0d36-4218-afe9-0a39f35b571d2024-03-27Warnings, Adverse reactionsExact identifier
application number: ANDA065169
ndc (package): 50090-0944-0
ndc (product): 50090-0944
rxcui: 1665005
spl id: aec67c2e-94ef-4be6-afb1-d5c47bbdfad1
spl set id: b642877e-0d36-4218-afe9-0a39f35b571d
unii: 023Z5BR09K
CeftriaxoneCEFTRIAXONECivica, Inc.96f3fc1e-84f4-4e9b-91ac-19a1692f227a2024-02-06Warnings, Adverse reactionsExact identifier
rxcui: 1665046
rxcui: 1665021
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMProficient Rx LP790279d4-2456-4091-abec-960b788854322024-02-01Warnings, Adverse reactionsExact identifier
rxcui: 1665005
unii: 023Z5BR09K

Reported adverse events (FAERS/openFDA)#

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