cefoxitin

Generic: cefoxitin

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

Drug Facts

Product Profile

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

cefoxitin sodium 10 g/1

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-111
Product ID 25021-111_79813968-4f6f-49a9-9a94-18607a1bcfbf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065415
Listing Expiration 2026-12-31
Marketing Start 2010-08-12

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021111
Hyphenated Format 25021-111

Supplemental Identifiers

RxCUI
309072
UNII
Q68050H03T

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 cefoxitin (source: ndc)
Generic Name cefoxitin (source: ndc)
Application Number ANDA065415 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 g/1
source: ndc
Packaging
  • 10 BOTTLE in 1 CARTON (25021-111-99) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE
source: ndc

Packages (1)

25021-111-99 10 BOTTLE in 1 CARTON (25021-111-99) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE

Ingredients (1)

cefoxitin sodium (10 g/1)

Linked Drug Pages (1)

Cefoxitin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "79813968-4f6f-49a9-9a94-18607a1bcfbf", "openfda": {"unii": ["Q68050H03T"], "rxcui": ["309072"], "spl_set_id": ["4c6f7665-204f-6c69-7669-61204d756e6e"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BOTTLE in 1 CARTON (25021-111-99)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE", "package_ndc": "25021-111-99", "marketing_start_date": "20100812"}], "brand_name": "Cefoxitin", "product_id": "25021-111_79813968-4f6f-49a9-9a94-18607a1bcfbf", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "25021-111", "generic_name": "cefoxitin", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefoxitin", "active_ingredients": [{"name": "CEFOXITIN SODIUM", "strength": "10 g/1"}], "application_number": "ANDA065415", "marketing_category": "ANDA", "marketing_start_date": "20100812", "listing_expiration_date": "20261231"}