CEFTRIAXONE
Ceftriaxone for injection, USP Rx only
Approved
Approval ID
1781fc07-5a2a-4b31-aad9-d0457eb704f4
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 9, 2012
Manufacturers
FDA
Rebel Distributors Corp
DUNS: 118802834
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 Code42254-152
Application NumberANDA065391
Product Classification
M
Marketing Category
C73584
G
Generic Name
CEFTRIAXONE
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
Effective DateFebruary 29, 2012
FDA Product Classification
INGREDIENTS (1)
CEFTRIAXONE SODIUMActive
Quantity: 500 mg in 1 1
Code: 023Z5BR09K
Classification: ACTIM