Cefazolin
Cefazolin for Injection, USP
Approved
Approval ID
d24529e3-e2b4-46d6-81ba-b7da74501792
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 1, 2022
Manufacturers
FDA
Proficient Rx LP
DUNS: 079196022
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 Code71205-679
Application NumberANDA203661
Product Classification
M
Marketing Category
C73584
G
Generic Name
Cefazolin
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
Effective DateAugust 1, 2022
FDA Product Classification
INGREDIENTS (1)
Cefazolin SodiumActive
Quantity: 1 g in 1 1
Code: P380M0454Z
Classification: ACTIM