cefoxitin

Generic: cefoxitin

Labeler: samson medical technologies llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefoxitin
Generic Name cefoxitin
Labeler samson medical technologies llc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

cefoxitin sodium 100 g/1

Manufacturer
SAMSON MEDICAL TECHNOLOGIES LLC

Identifiers & Regulatory

Product NDC 66288-4100
Product ID 66288-4100_b137208d-8dfd-4133-94c2-7287866a5525
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200938
Listing Expiration 2026-12-31
Marketing Start 2016-03-01

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 662884100
Hyphenated Format 66288-4100

Supplemental Identifiers

RxCUI
1739890
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 ANDA200938 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 g/1
source: ndc
Packaging
  • 1 BAG in 1 BAG (66288-4100-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BAG
source: ndc

Packages (1)

Ingredients (1)

cefoxitin sodium (100 g/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b137208d-8dfd-4133-94c2-7287866a5525", "openfda": {"unii": ["Q68050H03T"], "rxcui": ["1739890"], "spl_set_id": ["ea6dba56-5d9c-463a-b1d9-f7af5b602ed9"], "manufacturer_name": ["SAMSON MEDICAL TECHNOLOGIES LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BAG in 1 BAG (66288-4100-1)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 BAG", "package_ndc": "66288-4100-1", "marketing_start_date": "20160301"}], "brand_name": "Cefoxitin", "product_id": "66288-4100_b137208d-8dfd-4133-94c2-7287866a5525", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "66288-4100", "generic_name": "cefoxitin", "labeler_name": "SAMSON MEDICAL TECHNOLOGIES LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefoxitin", "active_ingredients": [{"name": "CEFOXITIN SODIUM", "strength": "100 g/1"}], "application_number": "ANDA200938", "marketing_category": "ANDA", "marketing_start_date": "20160301", "listing_expiration_date": "20261231"}