Oxacillin
Oxacillin for Injection, USP(For Intravenous or Intramuscular Injection)
Approved
Approval ID
c4c9bc2d-fe19-4aca-8042-42394d3a3510
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 10, 2018
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 Code25021-162
Application NumberANDA091246
Product Classification
M
Marketing Category
C73584
G
Generic Name
oxacillin sodium
Product Specifications
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateSeptember 10, 2018
FDA Product Classification
INGREDIENTS (2)
oxacillin sodiumActive
Quantity: 2 g in 1 1
Code: G0V6C994Q5
Classification: ACTIM
sodium phosphate, dibasicInactive
Code: GR686LBA74
Classification: IACT