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, FILM COATED
Routes
ORAL
Active Ingredients

cefuroxime axetil 250 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2159
Product ID 50090-2159_16361438-6bf9-42ee-93e0-1cda506d9bd3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065496
Listing Expiration 2026-12-31
Marketing Start 2010-12-01

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902159
Hyphenated Format 50090-2159

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 ANDA065496 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-2159-0)
  • 14 TABLET, FILM COATED in 1 BOTTLE (50090-2159-1)
source: ndc

Packages (2)

50090-2159-0 20 TABLET, FILM COATED in 1 BOTTLE (50090-2159-0) 50090-2159-1 14 TABLET, FILM COATED in 1 BOTTLE (50090-2159-1)

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": "16361438-6bf9-42ee-93e0-1cda506d9bd3", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309097"], "spl_set_id": ["84593261-838c-433a-8d9d-1d37b11058da"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-2159-0)", "package_ndc": "50090-2159-0", "marketing_start_date": "20151021"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-2159-1)", "package_ndc": "50090-2159-1", "marketing_start_date": "20240826"}], "brand_name": "Cefuroxime axetil", "product_id": "50090-2159_16361438-6bf9-42ee-93e0-1cda506d9bd3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-2159", "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": "ANDA065496", "marketing_category": "ANDA", "marketing_start_date": "20101201", "listing_expiration_date": "20261231"}