Package 70518-3215-3

Brand: Cefuroxime Axetil

Generic: Cefuroxime Axetil
NDC Package

Package Facts

Identity

Package NDC 70518-3215-3
Digits Only 7051832153
Product NDC 70518-3215
Product ID 70518-3215_3a349423-8a88-bf27-e063-6394a90ad156
Description

20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3215-3)

Marketing

Marketing Status
Marketed Since 2023-10-30
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": "3a349423-8a88-bf27-e063-6394a90ad156", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309098"], "spl_set_id": ["76cec54f-d167-4298-951b-5411a3c47f4a"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3215-3)", "package_ndc": "70518-3215-3", "marketing_start_date": "20231030"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3215-4)", "package_ndc": "70518-3215-4", "marketing_start_date": "20240113"}], "brand_name": "Cefuroxime Axetil", "product_id": "70518-3215_3a349423-8a88-bf27-e063-6394a90ad156", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "70518-3215", "generic_name": "Cefuroxime Axetil", "labeler_name": "REMEDYREPACK 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": "20210908", "listing_expiration_date": "20261231"}