Package 68071-3899-4

Brand: cefuroxime axetil

Generic: cefuroxime axetil
NDC Package

Package Facts

Identity

Package NDC 68071-3899-4
Digits Only 6807138994
Product NDC 68071-3899
Product ID 68071-3899_3f92c452-18b5-5af8-e063-6394a90aaa53
Description

14 TABLET, FILM COATED in 1 BOTTLE (68071-3899-4)

Marketing

Marketing Status
Marketed Since 2025-09-24
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": "3f92c452-18b5-5af8-e063-6394a90aaa53", "openfda": {"upc": ["0368071389944"], "unii": ["Z49QDT0J8Z"], "rxcui": ["309098"], "spl_set_id": ["3f92c452-18b4-5af8-e063-6394a90aaa53"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (68071-3899-4)", "package_ndc": "68071-3899-4", "marketing_start_date": "20250924"}], "brand_name": "Cefuroxime Axetil", "product_id": "68071-3899_3f92c452-18b5-5af8-e063-6394a90aaa53", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68071-3899", "generic_name": "Cefuroxime Axetil", "labeler_name": "NuCare Pharmaceuticals, Inc.", "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": "20060329", "listing_expiration_date": "20261231"}