CEFTRIAXONE
Ceftriaxone for Injection, USP
Approved
Approval ID
3b36beb7-db94-4b07-8c81-bd2b601a6601
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 2, 2015
Manufacturers
FDA
Wockhardt Limited
DUNS: 650069115
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 Code55648-703
Application NumberANDA065391
Product Classification
M
Marketing Category
C73584
G
Generic Name
CEFTRIAXONE
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
Effective DateSeptember 2, 2015
FDA Product Classification
INGREDIENTS (1)
CEFTRIAXONE SODIUMActive
Quantity: 2 g in 1 1
Code: 023Z5BR09K
Classification: ACTIM