Ceftriaxone
Ceftriaxone for Injection, USP
Approved
Approval ID
7bed9b33-29e3-4f04-9766-43a21c7ad47a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 24, 2023
Manufacturers
FDA
WG Critical Care, LLC
DUNS: 829274633
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ceftriaxone
PRODUCT DETAILS
NDC Product Code44567-702
Application NumberANDA065329
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 24, 2023
Generic NameCeftriaxone
INGREDIENTS (2)
CEFTRIAXONE SODIUMActive
Quantity: 2 g in 1 1
Code: 023Z5BR09K
Classification: ACTIM
NATURAL LATEX RUBBERInactive
Quantity: 0 1 in 1 1
Code: 2LQ0UUW8IN
Classification: CNTM
Ceftriaxone
PRODUCT DETAILS
NDC Product Code44567-701
Application NumberANDA065329
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 24, 2023
Generic NameCeftriaxone
INGREDIENTS (2)
CEFTRIAXONE SODIUMActive
Quantity: 1 g in 1 1
Code: 023Z5BR09K
Classification: ACTIM
NATURAL LATEX RUBBERInactive
Quantity: 0 1 in 1 1
Code: 2LQ0UUW8IN
Classification: CNTM