Package 67046-1081-3

Brand: cefuroxime axetil

Generic: cefuroxime axetil
NDC Package

Package Facts

Identity

Package NDC 67046-1081-3
Digits Only 6704610813
Product NDC 67046-1081
Product ID 67046-1081_2c3a51b0-6e4a-9ae0-e063-6394a90acc40
Description

30 TABLET in 1 BLISTER PACK (67046-1081-3)

Marketing

Marketing Status
Marketed Since 2025-01-21
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": "2c3a51b0-6e4a-9ae0-e063-6394a90acc40", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309098"], "spl_set_id": ["2c3a502f-8e72-c4d2-e063-6394a90a6fa5"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1081-3)", "package_ndc": "67046-1081-3", "marketing_start_date": "20250121"}], "brand_name": "Cefuroxime Axetil", "product_id": "67046-1081_2c3a51b0-6e4a-9ae0-e063-6394a90acc40", "dosage_form": "TABLET", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67046-1081", "generic_name": "Cefuroxime Axetil", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefuroxime Axetil", "active_ingredients": [{"name": "CEFUROXIME AXETIL", "strength": "500 mg/1"}], "application_number": "ANDA065308", "marketing_category": "ANDA", "marketing_start_date": "20250121", "listing_expiration_date": "20261231"}