Package 50090-2157-0

Brand: cefuroxime axetil

Generic: cefuroxime axetil
NDC Package

Package Facts

Identity

Package NDC 50090-2157-0
Digits Only 5009021570
Product NDC 50090-2157
Description

20 TABLET, FILM COATED in 1 BOTTLE (50090-2157-0)

Marketing

Marketing Status
Marketed Since 2015-10-21
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": "4c85dedc-e76f-40fb-bad7-99d7a2146679", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309097", "309098"], "spl_set_id": ["c89e8f4d-96c0-44c6-906a-b803141920b1"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-2157-0)", "package_ndc": "50090-2157-0", "marketing_start_date": "20151021"}], "brand_name": "Cefuroxime axetil", "product_id": "50090-2157_4c85dedc-e76f-40fb-bad7-99d7a2146679", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-2157", "generic_name": "Cefuroxime axetil", "labeler_name": "A-S Medication Solutions", "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"}