cefuroxime and dextrose
Generic: cefuroxime and dextrose
Labeler: b. braun medical inc.Drug Facts
Product Profile
Brand Name
cefuroxime and dextrose
Generic Name
cefuroxime and dextrose
Labeler
b. braun medical inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
cefuroxime sodium 1.5 g/50mL
Manufacturer
Identifiers & Regulatory
Product NDC
0264-3114
Product ID
0264-3114_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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02643114
Hyphenated Format
0264-3114
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
cefuroxime and dextrose (source: ndc)
Generic Name
cefuroxime and dextrose (source: ndc)
Application Number
NDA050780 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.5 g/50mL
Packaging
- 24 CONTAINER in 1 CASE (0264-3114-11) / 50 mL in 1 CONTAINER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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 (0264-3114-11) / 50 mL in 1 CONTAINER", "package_ndc": "0264-3114-11", "marketing_start_date": "20010221"}], "brand_name": "Cefuroxime and Dextrose", "product_id": "0264-3114_6874a295-7ec7-4822-9d04-4dd9932b4546", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0264-3114", "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": "1.5 g/50mL"}], "application_number": "NDA050780", "marketing_category": "NDA", "marketing_start_date": "20010221", "listing_expiration_date": "20261231"}