cefuroxime and dextrose

Generic: cefuroxime and dextrose

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

Drug Facts

Product Profile

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

cefuroxime sodium 750 mg/50mL

Manufacturer
B. Braun Medical Inc.

Identifiers & Regulatory

Product NDC 0264-3112
Product ID 0264-3112_6874a295-7ec7-4822-9d04-4dd9932b4546
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA050780
Listing Expiration 2026-12-31
Marketing Start 2001-02-21

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02643112
Hyphenated Format 0264-3112

Supplemental Identifiers

RxCUI
1665444 1665449
UNII
R8A7M9MY61

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 cefuroxime and dextrose (source: ndc)
Generic Name cefuroxime and dextrose (source: ndc)
Application Number NDA050780 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 750 mg/50mL
source: ndc
Packaging
  • 24 CONTAINER in 1 CASE (0264-3112-11) / 50 mL in 1 CONTAINER
source: ndc

Packages (1)

0264-3112-11 24 CONTAINER in 1 CASE (0264-3112-11) / 50 mL in 1 CONTAINER

Ingredients (1)

cefuroxime sodium (750 mg/50mL)

Linked Drug Pages (1)

Cefuroxime and Dextrose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "6874a295-7ec7-4822-9d04-4dd9932b4546", "openfda": {"unii": ["R8A7M9MY61"], "rxcui": ["1665444", "1665449"], "spl_set_id": ["07170ee3-1a24-424f-a2a2-00bc92e98f85"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 CONTAINER in 1 CASE (0264-3112-11)  / 50 mL in 1 CONTAINER", "package_ndc": "0264-3112-11", "marketing_start_date": "20010221"}], "brand_name": "Cefuroxime and Dextrose", "product_id": "0264-3112_6874a295-7ec7-4822-9d04-4dd9932b4546", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0264-3112", "generic_name": "CEFUROXIME AND DEXTROSE", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefuroxime and Dextrose", "active_ingredients": [{"name": "CEFUROXIME SODIUM", "strength": "750 mg/50mL"}], "application_number": "NDA050780", "marketing_category": "NDA", "marketing_start_date": "20010221", "listing_expiration_date": "20261231"}