Ceftriaxone
These highlights do not include all the information needed to use CEFTRIAXONE FOR INJECTION safely and effectively. See full prescribing information for CEFTRIAXONE FOR INJECTION. CEFTRIAXONE FOR INJECTION, USP Ceftriaxone for Injection, for intravenous use Initial U.S. Approval: 1984
Approved
Approval ID
5cd2d96f-83e5-4326-ae87-d0ede4ba493a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 15, 2023
Manufacturers
FDA
Samson Medical Technologies, LLC
DUNS: 102837429
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ceftriaxone Sodium
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code66288-6100
Application NumberANDA090057
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ceftriaxone Sodium
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJune 7, 2016
FDA Product Classification
INGREDIENTS (1)
CEFTRIAXONE SODIUMActive
Quantity: 100 g in 1 1
Code: 023Z5BR09K
Classification: ACTIM