Cefazolin
CEFAZOLIN FOR INJECTION, USP
Approved
Approval ID
570d2583-9ce7-4941-bf7c-6ebc783c0f2b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 15, 2018
Manufacturers
FDA
West-Ward Pharmaceuticals Corp
DUNS: 001230762
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 Code0143-9261
Application NumberANDA065143
Product Classification
M
Marketing Category
C73584
G
Generic Name
Cefazolin
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateSeptember 17, 2018
FDA Product Classification
INGREDIENTS (1)
CEFAZOLIN SODIUMActive
Quantity: 10 g in 1 1
Code: P380M0454Z
Classification: ACTIM