Package 0781-3207-95

Brand: ceftriaxone sodium

Generic: ceftriaxone sodium
NDC Package

Package Facts

Identity

Package NDC 0781-3207-95
Digits Only 0781320795
Product NDC 0781-3207
Description

10 VIAL, SINGLE-USE in 1 CARTON (0781-3207-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2005-05-09
Brand ceftriaxone sodium
Generic ceftriaxone sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "371d8db2-5d67-4339-92b7-aee2a52b2293", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["309092", "1665005", "1665021", "1665046"], "spl_set_id": ["de028434-46cf-44f6-8ac6-889c7c6943b3"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (0781-3207-85)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "0781-3207-85", "marketing_start_date": "20050509"}, {"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (0781-3207-95)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "0781-3207-95", "marketing_start_date": "20050509"}], "brand_name": "Ceftriaxone Sodium", "product_id": "0781-3207_371d8db2-5d67-4339-92b7-aee2a52b2293", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0781-3207", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Sandoz Inc", "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"}