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
NDC Product Code0409-7334
Application NumberANDA065168
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS
Effective DateJune 12, 2017
Generic NameCeftriaxone Sodium
INGREDIENTS (1)
CEFTRIAXONE SODIUMActive
Quantity: 10 g in 100 mL
Code: 023Z5BR09K
Classification: ACTIM