Package 67296-2168-7

Brand: cefuroxime axetil

Generic: cefuroxime axetil
NDC Package

Package Facts

Identity

Package NDC 67296-2168-7
Digits Only 6729621687
Product NDC 67296-2168
Product ID 67296-2168_45abddff-8c57-a374-e063-6294a90a83ea
Description

14 TABLET, FILM COATED in 1 BOTTLE (67296-2168-7)

Marketing

Marketing Status
Marketed Since 2010-12-01
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": "45abddff-8c57-a374-e063-6294a90a83ea", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309098"], "spl_set_id": ["3744f28c-c7e1-259c-e063-6294a90a10ed"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (67296-2168-7)", "package_ndc": "67296-2168-7", "marketing_start_date": "20101201"}], "brand_name": "Cefuroxime axetil", "product_id": "67296-2168_45abddff-8c57-a374-e063-6294a90a83ea", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67296-2168", "generic_name": "Cefuroxime axetil", "labeler_name": "Redpharm Drug", "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": "20101201", "listing_expiration_date": "20261231"}