Oxacillin
Oxacillin for Injection, USP For Intramuscular or Intravenous Injection
Approved
Approval ID
8e99d6fe-42ab-44c1-8b51-e4ac7406dbe4
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 3, 2024
Manufacturers
FDA
Armas Pharmaceuticals Inc.
DUNS: 098405973
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Oxacillin
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72485-409
Application NumberANDA091486
Product Classification
M
Marketing Category
C73584
G
Generic Name
Oxacillin
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
Effective DateJanuary 3, 2024
FDA Product Classification
INGREDIENTS (2)
SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORMInactive
Code: GR686LBA74
Classification: IACT
OXACILLIN SODIUMActive
Quantity: 2 g in 1 1
Code: G0V6C994Q5
Classification: ACTIM