Cefazolin
Cefazolin for Injection, USP
Approved
Approval ID
62441488-fc97-4535-a249-4485fb075022
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 8, 2020
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.
Cefazolin
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0409-2585
Application NumberANDA065345
Product Classification
M
Marketing Category
C73584
G
Generic Name
Cefazolin
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJune 15, 2017
FDA Product Classification
INGREDIENTS (1)
CEFAZOLIN SODIUMActive
Quantity: 1 g in 1 1
Code: P380M0454Z
Classification: ACTIM