cefuroxime axetil
Generic: cefuroxime axetil
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
cefuroxime axetil
Generic Name
cefuroxime axetil
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
cefuroxime axetil 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-4947
Product ID
68071-4947_1b2e322e-13be-c58d-e063-6394a90a2829
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065496
Listing Expiration
2026-12-31
Marketing Start
2010-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680714947
Hyphenated Format
68071-4947
Supplemental Identifiers
RxCUI
UPC
UNII
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 axetil (source: ndc)
Generic Name
cefuroxime axetil (source: ndc)
Application Number
ANDA065496 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 2 TABLET, FILM COATED in 1 BOTTLE (68071-4947-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b2e322e-13be-c58d-e063-6394a90a2829", "openfda": {"upc": ["0368071494723"], "unii": ["Z49QDT0J8Z"], "rxcui": ["309097"], "spl_set_id": ["8c3c1c85-cbce-66e2-e053-2a95a90a94fe"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (68071-4947-2)", "package_ndc": "68071-4947-2", "marketing_start_date": "20190626"}], "brand_name": "Cefuroxime axetil", "product_id": "68071-4947_1b2e322e-13be-c58d-e063-6394a90a2829", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68071-4947", "generic_name": "Cefuroxime axetil", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefuroxime axetil", "active_ingredients": [{"name": "CEFUROXIME AXETIL", "strength": "250 mg/1"}], "application_number": "ANDA065496", "marketing_category": "ANDA", "marketing_start_date": "20101201", "listing_expiration_date": "20261231"}