cefuroxime sodium

Generic: cefuroxime sodium

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefuroxime sodium
Generic Name cefuroxime sodium
Labeler sagent pharmaceuticals
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

cefuroxime sodium 750 mg/1

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-118
Product ID 25021-118_244117cb-7dfb-44fd-a670-323aae6b51f7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA064125
Listing Expiration 2026-12-31
Marketing Start 2016-09-01

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021118
Hyphenated Format 25021-118

Supplemental Identifiers

RxCUI
1665444 1665449
UNII
R8A7M9MY61

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cefuroxime sodium (source: ndc)
Generic Name cefuroxime sodium (source: ndc)
Application Number ANDA064125 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (25021-118-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
source: ndc

Packages (1)

25021-118-10 25 VIAL in 1 CARTON (25021-118-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

Ingredients (1)

cefuroxime sodium (750 mg/1)

Linked Drug Pages (1)

Cefuroxime sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "244117cb-7dfb-44fd-a670-323aae6b51f7", "openfda": {"unii": ["R8A7M9MY61"], "rxcui": ["1665444", "1665449"], "spl_set_id": ["0a145288-733a-4966-b7ae-dc96eb103d8c"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-118-10)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "25021-118-10", "marketing_start_date": "20160901"}], "brand_name": "Cefuroxime sodium", "product_id": "25021-118_244117cb-7dfb-44fd-a670-323aae6b51f7", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "25021-118", "generic_name": "Cefuroxime sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefuroxime sodium", "active_ingredients": [{"name": "CEFUROXIME SODIUM", "strength": "750 mg/1"}], "application_number": "ANDA064125", "marketing_category": "ANDA", "marketing_start_date": "20160901", "listing_expiration_date": "20261231"}