Package 50090-1875-0

Brand: ceftriaxone sodium

Generic: ceftriaxone sodium
NDC Package

Package Facts

Identity

Package NDC 50090-1875-0
Digits Only 5009018750
Product NDC 50090-1875
Product ID 50090-1875_48bba686-fc8a-4b5c-97c8-45e926912fd7
Description

10 VIAL, SINGLE-USE in 1 CARTON (50090-1875-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2015-06-16
Brand ceftriaxone sodium
Generic ceftriaxone sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "48bba686-fc8a-4b5c-97c8-45e926912fd7", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["309092"], "spl_set_id": ["1aa0a4ee-1b39-4c3d-a7a3-33dded6fe28c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (50090-1875-0)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "50090-1875-0", "marketing_start_date": "20150616"}], "brand_name": "Ceftriaxone Sodium", "product_id": "50090-1875_48bba686-fc8a-4b5c-97c8-45e926912fd7", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-1875", "generic_name": "Ceftriaxone Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA065169", "marketing_category": "ANDA", "marketing_start_date": "20050509", "listing_expiration_date": "20261231"}