NDC 66288-6100-01 - 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: 66288-6100
Requested NDC: 66288-6100-01
Package NDCs from labels: 66288-6100-1, 66288-6100-01
Manufacturer: Samson Medical Technologies, LLC | ACS Dobfar S.p.A.
Effective date: 2023-01-15
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Ceftriaxone - Samson Medical Technologies, LLC \| ACS Dobfar S.p.A.	Samson Medical Technologies, LLC \| ACS Dobfar S.p.A.	2023-01-15	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
66288-6100-1	Ceftriaxone	1 in 1 BAG	INJECTION, POWDER, FOR SOLUTION	1		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
66288-6100	CEFTRIAXONE (CEFTRIAXONE SODIUM) INJECTION, POWDER, FOR SOLUTION [SAMSON MEDICAL TECHNOLOGIES, LLC]	5	Current NDC, Legacy NDC, 1 package rows	20230116_5cd2d96f-83e5-4326-ae87-d0ede4ba493a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
66288-6100-1	EA - Each	66288-6100	6cc3300d-7e90-4977-9105-d62aa9c7d1ce	1	2015-10-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
CEFTRIAXONE SODIUM	ACTIVE INGREDIENT	023Z5BR09K	CEFTRIAXONE (CEFTRIAXONE SODIUM) INJECTION, POWDER, FOR SOLUTION [SAMSON MEDICAL TECHNOLOGIES, LLC]	1
CEFTRIAXONE	ACTIVE MOIETY	75J73V1629	CEFTRIAXONE (CEFTRIAXONE SODIUM) INJECTION, POWDER, FOR SOLUTION [SAMSON MEDICAL TECHNOLOGIES, LLC]	1

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 · 34 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ceftriaxone Sodium	CEFTRIAXONE SODIUM	A-S Medication Solutions	1aa0a4ee-1b39-4c3d-a7a3-33dded6fe28c	2024-01-31	Warnings, Adverse reactions	Exact identifier unii: 023Z5BR09K
Ceftriaxone Sodium	CEFTRIAXONE SODIUM	A-S Medication Solutions	ff8e830a-c288-46fb-9e19-ec2017943c07	2024-01-31	Warnings, Adverse reactions	Exact identifier unii: 023Z5BR09K
ceftriaxone	CEFTRIAXONE	Sagent Pharmaceuticals	5cf93bc5-9e4c-4734-bc02-c7d0ac071022	2023-11-08	Warnings, Adverse reactions	Exact identifier unii: 023Z5BR09K
Ceftriaxone	CEFTRIAXONE	Fresenius Kabi USA, LLC	7ea1db43-40fa-417b-8911-ae98092070a0	2023-09-30	Warnings, Adverse reactions	Exact identifier unii: 023Z5BR09K
Ceftriaxone Sodium	CEFTRIAXONE SODIUM	Asclemed USA, Inc.	f01cf0e5-caaf-4759-ba21-50f3aceff523	2023-09-02	Warnings, Adverse reactions	Exact identifier unii: 023Z5BR09K
Ceftriaxone Sodium	CEFTRIAXONE SODIUM	Apotex Corp.	5116231f-82d1-44be-b08e-560c9a50e5c5	2023-08-31	Warnings, Adverse reactions	Exact identifier unii: 023Z5BR09K
Ceftriaxone Sodium	CEFTRIAXONE SODIUM	Apotex Corp.	ac03a72c-0e35-40f9-b7fc-081badb5f19c	2023-01-28	Warnings, Adverse reactions	Exact identifier rxcui: 309090 unii: 023Z5BR09K
Ceftriaxone	CEFTRIAXONE SODIUM	Samson Medical Technologies, LLC	5cd2d96f-83e5-4326-ae87-d0ede4ba493a	2023-01-15	Warnings, Adverse reactions	Exact identifier application number: ANDA090057 ndc (package): 66288-6100-1 ndc (product): 66288-6100 ndc11 (package): 66288610001 rxcui: 309090 spl id: 6aff16e3-f491-4175-a3f2-842bed6ebecb spl set id: 5cd2d96f-83e5-4326-ae87-d0ede4ba493a unii: 023Z5BR09K
Ceftriaxone	CEFTRIAXONE	Proficient Rx LP	fcf401df-bcdc-4773-a63b-9741c0f74b3d	2022-11-01	Warnings, Adverse reactions	Exact identifier unii: 023Z5BR09K
Ceftriaxone Sodium	CEFTRIAXONE SODIUM	Proficient Rx LP	a25ab5ea-c46d-4562-8f7e-0ccffc2ab069	2022-10-01	Warnings, Adverse reactions	Exact identifier unii: 023Z5BR09K
Ceftriaxone Sodium	CEFTRIAXONE SODIUM	Proficient Rx LP	42ba7a9d-7d2b-4eac-af59-897151a8c924	2022-05-02	Warnings, Adverse reactions	Exact identifier unii: 023Z5BR09K
Ceftriaxone Sodium	CEFTRIAXONE SODIUM	Hospira, Inc	9d1f630b-e759-4395-9d01-ddc90e4fea75	2022-03-09	Warnings, Adverse reactions	Exact identifier unii: 023Z5BR09K
CEFTRIAXONE AND DEXTROSE	CEFTRIAXONE	B. Braun Medical Inc.	67153914-16bc-490d-82d7-638061618467	2022-01-13	Warnings, Adverse reactions	Exact identifier unii: 023Z5BR09K
Ceftriaxone	CEFTRIAXONE	Hikma Pharmaceuticals USA Inc.	1f8776bd-4f5b-427a-849a-6b8338f7997d	2019-04-24	Warnings, Adverse reactions	Exact identifier rxcui: 309090 unii: 023Z5BR09K

Reported adverse events (FAERS/openFDA)#

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