cefuroxime axetil

Generic: cefuroxime axetil

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefuroxime axetil
Generic Name cefuroxime axetil
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cefuroxime axetil 250 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0782
Product ID 50090-0782_20df5b5d-15b3-4fdb-9adc-e96174e43a3d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065308
Listing Expiration 2027-12-31
Marketing Start 2006-03-29

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500900782
Hyphenated Format 50090-0782

Supplemental Identifiers

RxCUI
309097
UNII
Z49QDT0J8Z

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (50090-0782-0)
  • 14 TABLET in 1 BOTTLE (50090-0782-1)
source: ndc

Packages (2)

50090-0782-0 20 TABLET in 1 BOTTLE (50090-0782-0) 50090-0782-1 14 TABLET in 1 BOTTLE (50090-0782-1)

Ingredients (1)

cefuroxime axetil (250 mg/1)

Linked Drug Pages (1)

Cefuroxime Axetil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "20df5b5d-15b3-4fdb-9adc-e96174e43a3d", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309097"], "spl_set_id": ["a940ba01-2b53-4947-9019-d3d8f4e9ad80"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-0782-0)", "package_ndc": "50090-0782-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (50090-0782-1)", "package_ndc": "50090-0782-1", "marketing_start_date": "20260119"}], "brand_name": "Cefuroxime Axetil", "product_id": "50090-0782_20df5b5d-15b3-4fdb-9adc-e96174e43a3d", "dosage_form": "TABLET", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-0782", "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": "20271231"}