Package 50090-0782-1

Brand: cefuroxime axetil

Generic: cefuroxime axetil
NDC Package

Package Facts

Identity

Package NDC 50090-0782-1
Digits Only 5009007821
Product NDC 50090-0782
Description

14 TABLET in 1 BOTTLE (50090-0782-1)

Marketing

Marketing Status
Marketed Since 2026-01-19
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": "20df5b5d-15b3-4fdb-9adc-e96174e43a3d", "openfda": {"unii": ["Z49QDT0J8Z"], "rxcui": ["309097"], "spl_set_id": ["a940ba01-2b53-4947-9019-d3d8f4e9ad80"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-0782-0)", "package_ndc": "50090-0782-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (50090-0782-1)", "package_ndc": "50090-0782-1", "marketing_start_date": "20260119"}], "brand_name": "Cefuroxime Axetil", "product_id": "50090-0782_20df5b5d-15b3-4fdb-9adc-e96174e43a3d", "dosage_form": "TABLET", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-0782", "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": "250 mg/1"}], "application_number": "ANDA065308", "marketing_category": "ANDA", "marketing_start_date": "20060329", "listing_expiration_date": "20271231"}