FDA.reportPublic FDA data

NDC 68330-005-01 - Ceftriaxone

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
68330-005
Requested NDC
68330-005-01
Package NDCs from labels
68330-005-01, 68330-005-10
Manufacturer
Cephazone Pharma LLC
Effective date
2012-09-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ceftriaxone - Cephazone Pharma LLCCephazone Pharma LLC2012-09-07HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unitNational Council for Prescription Drug Programs2013-02-13Indexing - Billing Unit

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68330-005-102019-11-13C16284748780-197449f38-ce81-f6ea-e053-dbdaa90aa703CEFTRIAXONE FOR INJECTION, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68330-005-01Ceftriaxone1 in 1 BOXINJECTION, POWDER, FOR SOLUTION12
68330-005-01Ceftriaxone1 in 1 VIAL, PIGGYBACKINJECTION, POWDER, FOR SOLUTION12
68330-005-10Ceftriaxone10 in 1 CARTONINJECTION, POWDER, FOR SOLUTION102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68330-005CEFTRIAXONE INJECTION, POWDER, FOR SOLUTION [CEPHAZONE PHARMA LLC]2Legacy NDC, 3 package rows20120908_e6ac87e3-481e-4884-ac06-1fd7279cad62.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68330-005-01EA - Each68330-00599fc54a3-135e-4d03-b2a6-ae2f155313f012013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CEFTRIAXONE SODIUMACTIVE INGREDIENT023Z5BR09KCEFTRIAXONE INJECTION, POWDER, FOR SOLUTION [CEPHAZONE PHARMA LLC]2
CEFTRIAXONEACTIVE MOIETY75J73V1629CEFTRIAXONE INJECTION, POWDER, FOR SOLUTION [CEPHAZONE PHARMA LLC]2

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 2 of 2 · 35 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ceftriaxone SodiumCEFTRIAXONE SODIUMA-S Medication Solutions1aa0a4ee-1b39-4c3d-a7a3-33dded6fe28c2024-01-31Warnings, Adverse reactionsExact identifier
rxcui: 309092
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMA-S Medication Solutionsff8e830a-c288-46fb-9e19-ec2017943c072024-01-31Warnings, Adverse reactionsExact identifier
rxcui: 309092
unii: 023Z5BR09K
ceftriaxoneCEFTRIAXONESagent Pharmaceuticals5cf93bc5-9e4c-4734-bc02-c7d0ac0710222023-11-08Warnings, Adverse reactionsExact identifier
rxcui: 1665046
rxcui: 1665005
rxcui: 1665021
unii: 023Z5BR09K
CeftriaxoneCEFTRIAXONEFresenius Kabi USA, LLC7ea1db43-40fa-417b-8911-ae98092070a02023-09-30Warnings, Adverse reactionsExact identifier
rxcui: 1665046
rxcui: 1665005
rxcui: 1665021
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMAsclemed USA, Inc.f01cf0e5-caaf-4759-ba21-50f3aceff5232023-09-02Warnings, Adverse reactionsExact identifier
rxcui: 1665005
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMApotex Corp.5116231f-82d1-44be-b08e-560c9a50e5c52023-08-31Warnings, Adverse reactionsExact identifier
rxcui: 1665046
rxcui: 1665005
rxcui: 309092
rxcui: 1665021
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMApotex Corp.ac03a72c-0e35-40f9-b7fc-081badb5f19c2023-01-28Warnings, Adverse reactionsExact identifier
unii: 023Z5BR09K
CeftriaxoneCEFTRIAXONE SODIUMSamson Medical Technologies, LLC5cd2d96f-83e5-4326-ae87-d0ede4ba493a2023-01-15Warnings, Adverse reactionsExact identifier
unii: 023Z5BR09K
CeftriaxoneCEFTRIAXONEProficient Rx LPfcf401df-bcdc-4773-a63b-9741c0f74b3d2022-11-01Warnings, Adverse reactionsExact identifier
rxcui: 1665046
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMProficient Rx LPa25ab5ea-c46d-4562-8f7e-0ccffc2ab0692022-10-01Warnings, Adverse reactionsExact identifier
rxcui: 1665046
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMProficient Rx LP42ba7a9d-7d2b-4eac-af59-897151a8c9242022-05-02Warnings, Adverse reactionsExact identifier
rxcui: 1665021
unii: 023Z5BR09K
Ceftriaxone SodiumCEFTRIAXONE SODIUMHospira, Inc9d1f630b-e759-4395-9d01-ddc90e4fea752022-03-09Warnings, Adverse reactionsExact identifier
rxcui: 1665046
rxcui: 1665021
unii: 023Z5BR09K
CEFTRIAXONE AND DEXTROSECEFTRIAXONEB. Braun Medical Inc.67153914-16bc-490d-82d7-6380616184672022-01-13Warnings, Adverse reactionsExact identifier
rxcui: 1665046
rxcui: 1665021
unii: 023Z5BR09K
CeftriaxoneCEFTRIAXONEHikma Pharmaceuticals USA Inc.1f8776bd-4f5b-427a-849a-6b8338f7997d2019-04-24Warnings, Adverse reactionsExact identifier
unii: 023Z5BR09K
4e15b344-d5b4-415b-8ce1-a856dc37a13ce6ac87e3-481e-4884-ac06-1fd7279cad622012-09-07Warnings, Adverse reactionsExact identifier
spl id: 4e15b344-d5b4-415b-8ce1-a856dc37a13c
spl set id: e6ac87e3-481e-4884-ac06-1fd7279cad62

Reported adverse events (FAERS/openFDA)#

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