Ceftriaxone
Ceftriaxone for Injection, USP
Approved
Approval ID
86ec0a92-a552-4a6d-9125-a54f95e43392
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 18, 2023
Manufacturers
FDA
WG Critical Care, LLC
DUNS: 829274633
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ceftriaxone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code44567-703
Application NumberANDA065328
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ceftriaxone
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateOctober 18, 2023
FDA Product Classification
INGREDIENTS (2)
CEFTRIAXONE SODIUMActive
Quantity: 10 g in 100 mL
Code: 023Z5BR09K
Classification: ACTIM
NATURAL LATEX RUBBERInactive
Quantity: 0 1 in 100 mL
Code: 2LQ0UUW8IN
Classification: CNTM