Package 63629-9447-1

Brand: cefuroxime axetil

Generic: cefuroxime axetil
NDC Package

Package Facts

Identity

Package NDC 63629-9447-1
Digits Only 6362994471
Product NDC 63629-9447
Description

60 TABLET, FILM COATED in 1 BOTTLE (63629-9447-1)

Marketing

Marketing Status
Marketed Since 2022-09-28
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": "165e0286-8087-41a5-861e-2776adc42fc4", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309097"], "spl_set_id": ["0d2a0215-efbb-4975-a2f6-fe32ae4d5cb2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63629-9447-1)", "package_ndc": "63629-9447-1", "marketing_start_date": "20220928"}], "brand_name": "Cefuroxime axetil", "product_id": "63629-9447_165e0286-8087-41a5-861e-2776adc42fc4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "63629-9447", "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": "250 mg/1"}], "application_number": "ANDA065496", "marketing_category": "ANDA", "marketing_start_date": "20101201", "listing_expiration_date": "20261231"}