Package 50090-0944-0

Brand: ceftriaxone sodium

Generic: ceftriaxone sodium
NDC Package

Package Facts

Identity

Package NDC 50090-0944-0
Digits Only 5009009440
Product NDC 50090-0944
Product ID 50090-0944_aec67c2e-94ef-4be6-afb1-d5c47bbdfad1
Description

10 VIAL, SINGLE-USE in 1 CARTON (50090-0944-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2014-11-28
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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "aec67c2e-94ef-4be6-afb1-d5c47bbdfad1", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["1665005"], "spl_set_id": ["b642877e-0d36-4218-afe9-0a39f35b571d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (50090-0944-0)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "50090-0944-0", "marketing_start_date": "20141128"}], "brand_name": "Ceftriaxone Sodium", "product_id": "50090-0944_aec67c2e-94ef-4be6-afb1-d5c47bbdfad1", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-0944", "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": "500 mg/1"}], "application_number": "ANDA065169", "marketing_category": "ANDA", "marketing_start_date": "20050509", "listing_expiration_date": "20261231"}