Package 0409-7333-04

Brand: ceftriaxone sodium

Generic: ceftriaxone sodium
NDC Package

Package Facts

Identity

Package NDC 0409-7333-04
Digits Only 0409733304
Product NDC 0409-7333
Product ID 0409-7333_8e4ee031-a0df-403f-8a7e-de9626a7e501
Description

10 VIAL, SINGLE-USE in 1 CARTON (0409-7333-04) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7333-11)

Marketing

Marketing Status
Discontinued 2027-03-31
Brand ceftriaxone sodium
Generic ceftriaxone sodium
Sample Package No

Linked Drug Pages (1)

Ceftriaxone Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "8e4ee031-a0df-403f-8a7e-de9626a7e501", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["1665021", "1665046"], "spl_set_id": ["128bb292-d174-4769-b3e6-9f16617f31e3"], "manufacturer_name": ["Hospira, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (0409-7333-04)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7333-11)", "package_ndc": "0409-7333-04", "marketing_end_date": "20270331", "marketing_start_date": "20050720"}], "brand_name": "Ceftriaxone Sodium", "product_id": "0409-7333_8e4ee031-a0df-403f-8a7e-de9626a7e501", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0409-7333", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Hospira, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "1 g/1"}], "application_number": "ANDA065204", "marketing_category": "ANDA", "marketing_end_date": "20270430", "marketing_start_date": "20050720"}