Cefazolin
CEFAZOLIN FOR INJECTION, USP
Approved
Approval ID
c24e604f-16ca-4945-8e9d-277cc67a8c68
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 25, 2022
Manufacturers
FDA
Civica, Inc.
DUNS: 081373942
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 Code72572-056
Application NumberANDA065143
Product Classification
M
Marketing Category
C73584
G
Generic Name
Cefazolin
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateFebruary 25, 2022
FDA Product Classification
INGREDIENTS (1)
CEFAZOLIN SODIUMActive
Quantity: 10 g in 1 1
Code: P380M0454Z
Classification: ACTIM