Package 0409-7333-49

Brand: ceftriaxone sodium

Generic: ceftriaxone sodium
NDC Package

Package Facts

Identity

Package NDC 0409-7333-49
Digits Only 0409733349
Product NDC 0409-7333
Product ID 0409-7333_f0a84916-b2bd-49eb-ab4b-dd7347445280
Description

10 VIAL, SINGLE-USE in 1 CARTON (0409-7333-49) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7333-31)

Marketing

Marketing Status
Marketed Since 2005-07-20
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": "f0a84916-b2bd-49eb-ab4b-dd7347445280", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["1665021", "1665046"], "spl_set_id": ["9d1f630b-e759-4395-9d01-ddc90e4fea75"], "manufacturer_name": ["Hospira, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (0409-7333-49)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7333-31)", "package_ndc": "0409-7333-49", "marketing_start_date": "20050720"}], "brand_name": "Ceftriaxone Sodium", "product_id": "0409-7333_f0a84916-b2bd-49eb-ab4b-dd7347445280", "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_start_date": "20050714", "listing_expiration_date": "20261231"}