Package 80425-0571-1

Brand: cefuroxime axetil

Generic: cefuroxime axetil
NDC Package

Package Facts

Identity

Package NDC 80425-0571-1
Digits Only 8042505711
Product NDC 80425-0571
Product ID 80425-0571_48d96610-0a63-48c4-e063-6294a90a0388
Description

20 TABLET, FILM COATED in 1 BOTTLE (80425-0571-1)

Marketing

Marketing Status
Marketed Since 2026-01-16
Brand cefuroxime axetil
Generic cefuroxime axetil
Sample Package No

Linked Drug Pages (1)

Cefuroxime axetil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48d96610-0a63-48c4-e063-6294a90a0388", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309098"], "spl_set_id": ["48d96608-d3da-b512-e063-6294a90a07d5"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (80425-0571-1)", "package_ndc": "80425-0571-1", "marketing_start_date": "20260116"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0571-2)", "package_ndc": "80425-0571-2", "marketing_start_date": "20260116"}], "brand_name": "Cefuroxime axetil", "product_id": "80425-0571_48d96610-0a63-48c4-e063-6294a90a0388", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "80425-0571", "generic_name": "Cefuroxime axetil", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefuroxime axetil", "active_ingredients": [{"name": "CEFUROXIME AXETIL", "strength": "500 mg/1"}], "application_number": "ANDA065496", "marketing_category": "ANDA", "marketing_start_date": "20260116", "listing_expiration_date": "20271231"}