cefoxitin
Generic: cefoxitin
Labeler: samson medical technologies llcDrug Facts
Product Profile
Brand Name
cefoxitin
Generic Name
cefoxitin
Labeler
samson medical technologies llc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cefoxitin sodium 100 g/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
662884100
Hyphenated Format
66288-4100
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 100 g/1
Packaging
- 1 BAG in 1 BAG (66288-4100-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BAG
Packages (1)
Ingredients (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"}