Oxacillin
Oxacillin for Injection, USP
Approved
Approval ID
9f0f30cb-ade2-4690-b63d-b069b8e4ed89
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 5, 2020
Manufacturers
FDA
Sagent Pharmaceuticals
DUNS: 796852890
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 Code25021-163
Application NumberANDA091245
Product Classification
M
Marketing Category
C73584
G
Generic Name
oxacillin sodium
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateMay 5, 2020
FDA Product Classification
INGREDIENTS (2)
oxacillin sodiumActive
Quantity: 10 g in 100 mL
Code: G0V6C994Q5
Classification: ACTIM
sodium phosphate, dibasic, unspecified formInactive
Code: GR686LBA74
Classification: IACT