CEFAZOLIN
These highlights do not include all the information needed to use Cefazolin for Injection, USP safely and effectively. See full prescribing information for Cefazolin for Injection, USP.CEFAZOLIN FOR INJECTION, USPInitial U.S. Approval: 1973
Approved
Approval ID
cf13db9c-d8a1-489f-9aa0-fc70839d4bbc
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 8, 2020
Manufacturers
FDA
Samson Medical Technologies, L.L.C.
DUNS: 102837429
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
CEFAZOLIN SODIUM
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code66288-1100
Application NumberANDA065141
Product Classification
M
Marketing Category
C73584
G
Generic Name
CEFAZOLIN SODIUM
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateOctober 24, 2018
FDA Product Classification
INGREDIENTS (1)
Cefazolin SodiumActive
Quantity: 100 g in 1 1
Code: P380M0454Z
Classification: ACTIM
CEFAZOLIN SODIUM
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code66288-1300
Application NumberANDA065141
Product Classification
M
Marketing Category
C73584
G
Generic Name
CEFAZOLIN SODIUM
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateOctober 24, 2018
FDA Product Classification
INGREDIENTS (1)
Cefazolin SodiumActive
Quantity: 300 g in 1 1
Code: P380M0454Z
Classification: ACTIM