Package 0904-7542-10

Brand: cefuroxime axetil

Generic: cefuroxime axetil
NDC Package

Package Facts

Identity

Package NDC 0904-7542-10
Digits Only 0904754210
Product NDC 0904-7542
Product ID 0904-7542_8f3e739a-07d6-48a6-812f-49e049048bd3
Description

2 BLISTER PACK in 1 CARTON (0904-7542-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-08-25
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": "8f3e739a-07d6-48a6-812f-49e049048bd3", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309097"], "spl_set_id": ["44e1fb4d-4b61-40da-9974-0bd2006eb828"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0904-7542-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7542-10", "marketing_start_date": "20250825"}], "brand_name": "Cefuroxime axetil", "product_id": "0904-7542_8f3e739a-07d6-48a6-812f-49e049048bd3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0904-7542", "generic_name": "Cefuroxime axetil", "labeler_name": "Major Pharmaceuticals", "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": "20250825", "listing_expiration_date": "20261231"}