Ceftriaxone Sodium
Ceftriaxone for Injection, USP
Approved
Approval ID
365fc265-8e6c-432f-9fda-911f5f7fb451
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 15, 2022
Manufacturers
FDA
Hospira, Inc
DUNS: 141588017
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 Code0409-7334
Application NumberANDA065168
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ceftriaxone Sodium
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJune 12, 2017
FDA Product Classification
INGREDIENTS (1)
CEFTRIAXONE SODIUMActive
Quantity: 10 g in 100 mL
Code: 023Z5BR09K
Classification: ACTIM