Package 67046-1307-3
Brand: cefuroxime axetil
Generic: cefuroxime axetilPackage Facts
Identity
Package NDC
67046-1307-3
Digits Only
6704613073
Product NDC
67046-1307
Description
30 TABLET in 1 BLISTER PACK (67046-1307-3)
Marketing
Marketing Status
Brand
cefuroxime axetil
Generic
cefuroxime axetil
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c6191df-9524-9c51-e063-6294a90a236c", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309097"], "spl_set_id": ["2c619a79-6b69-b9fa-e063-6394a90a8f27"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1307-3)", "package_ndc": "67046-1307-3", "marketing_start_date": "20250123"}], "brand_name": "Cefuroxime Axetil", "product_id": "67046-1307_2c6191df-9524-9c51-e063-6294a90a236c", "dosage_form": "TABLET", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67046-1307", "generic_name": "Cefuroxime Axetil", "labeler_name": "Coupler LLC", "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": "20250123", "listing_expiration_date": "20261231"}