cefoxitin

Generic: cefoxitin sodium

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefoxitin
Generic Name cefoxitin sodium
Labeler fresenius kabi usa, llc
Dosage Form POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

cefoxitin sodium 2 g/1

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-342
Product ID 63323-342_9f457501-b963-49c0-89a3-4228eb493895
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065414
Listing Expiration 2026-12-31
Marketing Start 2011-07-06

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63323342
Hyphenated Format 63323-342

Supplemental Identifiers

RxCUI
1665102 1665107
UPC
0363323342012 0363323341015
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 sodium (source: ndc)
Application Number ANDA065414 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 g/1
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (63323-342-25) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-342-01)
source: ndc

Packages (1)

63323-342-25 25 VIAL in 1 CARTON (63323-342-25) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-342-01)

Ingredients (1)

cefoxitin sodium (2 g/1)

Linked Drug Pages (2)

Cefoxitin ndc-match (0.9) Cefoxitin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "9f457501-b963-49c0-89a3-4228eb493895", "openfda": {"upc": ["0363323342012", "0363323341015"], "unii": ["Q68050H03T"], "rxcui": ["1665102", "1665107"], "spl_set_id": ["d02170ff-65aa-48b8-a922-94271c46ffa7"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (63323-342-25)  / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-342-01)", "package_ndc": "63323-342-25", "marketing_start_date": "20110706"}], "brand_name": "Cefoxitin", "product_id": "63323-342_9f457501-b963-49c0-89a3-4228eb493895", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "63323-342", "generic_name": "Cefoxitin Sodium", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefoxitin", "active_ingredients": [{"name": "CEFOXITIN SODIUM", "strength": "2 g/1"}], "application_number": "ANDA065414", "marketing_category": "ANDA", "marketing_start_date": "20110706", "listing_expiration_date": "20261231"}