Cefotaxime
Cefotaxime for Injection, USP
Approved
Approval ID
ef1a6dc6-bc3d-4f09-8f92-7ff328f56561
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 15, 2018
Manufacturers
FDA
West-Ward Pharmaceuticals Corp
DUNS: 001230762
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Cefotaxime
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0143-9935
Application NumberANDA065071
Product Classification
M
Marketing Category
C73584
G
Generic Name
Cefotaxime
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateSeptember 17, 2018
FDA Product Classification
INGREDIENTS (1)
CEFOTAXIME SODIUMActive
Quantity: 10 g in 1 1
Code: 258J72S7TZ
Classification: ACTIM