Package 82804-066-10

Brand: ceftriaxone sodium

Generic: ceftriaxone sodium
NDC Package

Package Facts

Identity

Package NDC 82804-066-10
Digits Only 8280406610
Product NDC 82804-066
Product ID 82804-066_790279d4-2456-4091-abec-960b78885432
Description

10 VIAL, SINGLE-USE in 1 CARTON (82804-066-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2024-02-02
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": "790279d4-2456-4091-abec-960b78885432", "openfda": {"upc": ["0382804066018"], "unii": ["023Z5BR09K"], "rxcui": ["1665005"], "spl_set_id": ["790279d4-2456-4091-abec-960b78885432"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (82804-066-01)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "82804-066-01", "marketing_start_date": "20240202"}, {"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (82804-066-10)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "82804-066-10", "marketing_start_date": "20240202"}], "brand_name": "Ceftriaxone Sodium", "product_id": "82804-066_790279d4-2456-4091-abec-960b78885432", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "82804-066", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA203702", "marketing_category": "ANDA", "marketing_start_date": "20170630", "listing_expiration_date": "20261231"}