cefoxitin

Generic: cefoxitin

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefoxitin
Generic Name cefoxitin
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

cefoxitin sodium 1 g/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9878
Product ID 0143-9878_4638263b-1c03-4a32-ba82-70270cf42490
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065238
Listing Expiration 2026-12-31
Marketing Start 2010-03-12

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439878
Hyphenated Format 0143-9878

Supplemental Identifiers

RxCUI
1665102 1665107
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 ANDA065238 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (0143-9878-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9878-01)
source: ndc

Packages (1)

0143-9878-25 25 VIAL in 1 CARTON (0143-9878-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9878-01)

Ingredients (1)

cefoxitin sodium (1 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": "4638263b-1c03-4a32-ba82-70270cf42490", "openfda": {"unii": ["Q68050H03T"], "rxcui": ["1665102", "1665107"], "spl_set_id": ["d2c449b9-5624-4166-95b1-d7813b3d0445"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0143-9878-25)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9878-01)", "package_ndc": "0143-9878-25", "marketing_start_date": "20100312"}], "brand_name": "Cefoxitin", "product_id": "0143-9878_4638263b-1c03-4a32-ba82-70270cf42490", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9878", "generic_name": "Cefoxitin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefoxitin", "active_ingredients": [{"name": "CEFOXITIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA065238", "marketing_category": "ANDA", "marketing_start_date": "20100312", "listing_expiration_date": "20261231"}