Package 63629-9448-1

Brand: cefuroxime axetil

Generic: cefuroxime axetil
NDC Package

Package Facts

Identity

Package NDC 63629-9448-1
Digits Only 6362994481
Product NDC 63629-9448
Product ID 63629-9448_df6291c0-dfdd-4cd4-9e9c-e1c355cf1cd0
Description

20 TABLET, FILM COATED in 1 BOTTLE (63629-9448-1)

Marketing

Marketing Status
Marketed Since 2022-09-28
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": "df6291c0-dfdd-4cd4-9e9c-e1c355cf1cd0", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309098"], "spl_set_id": ["aa1c5720-b698-415f-997f-cbe4e35c69be"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (63629-9448-1)", "package_ndc": "63629-9448-1", "marketing_start_date": "20220928"}], "brand_name": "Cefuroxime axetil", "product_id": "63629-9448_df6291c0-dfdd-4cd4-9e9c-e1c355cf1cd0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "63629-9448", "generic_name": "Cefuroxime axetil", "labeler_name": "Bryant Ranch Prepack", "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"}