Package 0143-9678-01

Brand: ceftriaxone

Generic: ceftriaxone
NDC Package

Package Facts

Identity

Package NDC 0143-9678-01
Digits Only 0143967801
Product NDC 0143-9678
Product ID 0143-9678_e9f12b84-2885-442d-b53c-0fd5a9946d38
Description

1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (0143-9678-01)

Marketing

Marketing Status
Marketed Since 2017-10-04
Brand ceftriaxone
Generic ceftriaxone
Sample Package No

Linked Drug Pages (1)

Ceftriaxone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "e9f12b84-2885-442d-b53c-0fd5a9946d38", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["309090"], "spl_set_id": ["1f8776bd-4f5b-427a-849a-6b8338f7997d"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (0143-9678-01)", "package_ndc": "0143-9678-01", "marketing_start_date": "20171004"}], "brand_name": "Ceftriaxone", "product_id": "0143-9678_e9f12b84-2885-442d-b53c-0fd5a9946d38", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9678", "generic_name": "Ceftriaxone", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "10 g/1"}], "application_number": "ANDA090701", "marketing_category": "ANDA", "marketing_start_date": "20171004", "listing_expiration_date": "20261231"}