cefuroxime axetil
Generic: cefuroxime axetil
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
cefuroxime axetil
Generic Name
cefuroxime axetil
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
cefuroxime axetil 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6999
Product ID
50090-6999_13ec0bb9-d5aa-4e86-91e2-3be896570a4d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065308
Listing Expiration
2026-12-31
Marketing Start
2006-03-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906999
Hyphenated Format
50090-6999
Supplemental Identifiers
RxCUI
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
ANDA065308 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 20 TABLET in 1 BOTTLE (50090-6999-0)
- 14 TABLET in 1 BOTTLE (50090-6999-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "13ec0bb9-d5aa-4e86-91e2-3be896570a4d", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309097"], "spl_set_id": ["bcf7870a-7e45-4ae1-a9b4-457e4781886a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-6999-0)", "package_ndc": "50090-6999-0", "marketing_start_date": "20231227"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (50090-6999-1)", "package_ndc": "50090-6999-1", "marketing_start_date": "20240103"}], "brand_name": "Cefuroxime Axetil", "product_id": "50090-6999_13ec0bb9-d5aa-4e86-91e2-3be896570a4d", "dosage_form": "TABLET", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-6999", "generic_name": "Cefuroxime Axetil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefuroxime Axetil", "active_ingredients": [{"name": "CEFUROXIME AXETIL", "strength": "250 mg/1"}], "application_number": "ANDA065308", "marketing_category": "ANDA", "marketing_start_date": "20060329", "listing_expiration_date": "20261231"}