Package 70518-3215-4

Brand: cefuroxime axetil

Generic: cefuroxime axetil
NDC Package

Package Facts

Identity

Package NDC 70518-3215-4
Digits Only 7051832154
Product NDC 70518-3215
Product ID 70518-3215_4ab61a1a-01ab-1dfa-e063-6294a90a4d37
Description

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3215-4)

Marketing

Marketing Status
Marketed Since 2024-01-13
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": "4ab61a1a-01ab-1dfa-e063-6294a90a4d37", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309098"], "spl_set_id": ["76cec54f-d167-4298-951b-5411a3c47f4a"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"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_4ab61a1a-01ab-1dfa-e063-6294a90a4d37", "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": "20271231"}