CEFAZOLIN
Cefazolin for Injection, USP
Approved
Approval ID
5a8c4bb2-a75e-4d7d-91fb-9a95f04fc94b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 6, 2023
Manufacturers
FDA
Henry Schein, Inc.
DUNS: 012430880
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 Code0404-9833
Application NumberANDA203661
Product Classification
M
Marketing Category
C73584
G
Generic Name
cefazolin
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
Effective DateJanuary 9, 2022
FDA Product Classification
INGREDIENTS (1)
CEFAZOLIN SODIUMActive
Quantity: 1 g in 1 1
Code: P380M0454Z
Classification: ACTIM