Package 0143-9859-25
Brand: ceftriaxone
Generic: ceftriaxonePackage Facts
Identity
Package NDC
0143-9859-25
Digits Only
0143985925
Product NDC
0143-9859
Description
25 VIAL in 1 BOX (0143-9859-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9859-01)
Marketing
Marketing Status
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": "ff2e929e-05bc-4771-9af4-53b52acfd5bc", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["309092", "1665005", "1665021", "1665046"], "spl_set_id": ["8351aa37-552d-471d-b293-c564dcb6ec29"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 BOX (0143-9859-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9859-01)", "package_ndc": "0143-9859-25", "marketing_start_date": "20080110"}], "brand_name": "Ceftriaxone", "product_id": "0143-9859_ff2e929e-05bc-4771-9af4-53b52acfd5bc", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9859", "generic_name": "ceftriaxone", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA065342", "marketing_category": "ANDA", "marketing_start_date": "20080110", "listing_expiration_date": "20261231"}