cefoxitin and dextrose

Generic: cefoxitin sodium

Labeler: b. braun medical inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefoxitin and dextrose
Generic Name cefoxitin sodium
Labeler b. braun medical inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

cefoxitin sodium 1 g/50mL

Manufacturer
B. Braun Medical Inc.

Identifiers & Regulatory

Product NDC 0264-3123
Product ID 0264-3123_0cca0e6a-3047-4142-af33-d9b98efe85b1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA065214
Listing Expiration 2026-12-31
Marketing Start 2006-03-10

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02643123
Hyphenated Format 0264-3123

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 and dextrose (source: ndc)
Generic Name cefoxitin sodium (source: ndc)
Application Number NDA065214 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/50mL
source: ndc
Packaging
  • 24 CONTAINER in 1 CASE (0264-3123-11) / 50 mL in 1 CONTAINER
source: ndc

Packages (1)

0264-3123-11 24 CONTAINER in 1 CASE (0264-3123-11) / 50 mL in 1 CONTAINER

Ingredients (1)

cefoxitin sodium (1 g/50mL)

Linked Drug Pages (1)

Cefoxitin and Dextrose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "0cca0e6a-3047-4142-af33-d9b98efe85b1", "openfda": {"unii": ["Q68050H03T"], "rxcui": ["1665102", "1665107"], "spl_set_id": ["6c7e9485-1ede-411c-8c46-911439332864"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 CONTAINER in 1 CASE (0264-3123-11)  / 50 mL in 1 CONTAINER", "package_ndc": "0264-3123-11", "marketing_start_date": "20060310"}], "brand_name": "Cefoxitin and Dextrose", "product_id": "0264-3123_0cca0e6a-3047-4142-af33-d9b98efe85b1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0264-3123", "generic_name": "CEFOXITIN SODIUM", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefoxitin and Dextrose", "active_ingredients": [{"name": "CEFOXITIN SODIUM", "strength": "1 g/50mL"}], "application_number": "NDA065214", "marketing_category": "NDA", "marketing_start_date": "20060310", "listing_expiration_date": "20261231"}