Cefazolin
Approved
Approval ID
db977f52-2296-4003-9162-c155163d714a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 8, 2010
Manufacturers
FDA
Physicians Total Care, Inc.
DUNS: 194123980
Products 1
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 Code54868-4651
Application NumberANDA065047
Product Classification
M
Marketing Category
C73584
G
Generic Name
Cefazolin sodium
Product Specifications
Route of AdministrationINTRAMUSCULAR
Effective DateDecember 8, 2010
FDA Product Classification
INGREDIENTS (1)
CEFAZOLIN SODIUMActive
Quantity: 500 mg in 10 mL
Code: P380M0454Z
Classification: ACTIB