Package 72572-061-25

Brand: ceftriaxone

Generic: ceftriaxone
NDC Package

Package Facts

Identity

Package NDC 72572-061-25
Digits Only 7257206125
Product NDC 72572-061
Description

25 VIAL in 1 BOX (72572-061-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (72572-061-01)

Marketing

Marketing Status
Marketed Since 2020-03-01
Brand ceftriaxone
Generic ceftriaxone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "36b74132-c90c-4cda-bd0c-93855b45e205", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["1665021", "1665046"], "spl_set_id": ["96f3fc1e-84f4-4e9b-91ac-19a1692f227a"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 BOX (72572-061-25)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (72572-061-01)", "package_ndc": "72572-061-25", "marketing_start_date": "20200301"}], "brand_name": "Ceftriaxone", "product_id": "72572-061_36b74132-c90c-4cda-bd0c-93855b45e205", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "72572-061", "generic_name": "Ceftriaxone", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "1 g/1"}], "application_number": "ANDA065342", "marketing_category": "ANDA", "marketing_start_date": "20200301", "listing_expiration_date": "20261231"}