Oxacillin
Oxacillin for Injection, USP
Approved
Approval ID
152758c0-d225-4761-abeb-3f1cb0190806
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 10, 2022
Manufacturers
FDA
Eugia US LLC
DUNS: 968961354
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Oxacillin Sodium
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code55150-129
Application NumberANDA201538
Product Classification
M
Marketing Category
C73584
G
Generic Name
Oxacillin Sodium
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateFebruary 2, 2023
FDA Product Classification
INGREDIENTS (2)
OXACILLIN SODIUMActive
Quantity: 10 g in 100 mL
Code: G0V6C994Q5
Classification: ACTIM
SODIUM PHOSPHATE, DIBASICInactive
Code: GR686LBA74
Classification: IACT