ceftriaxone
Generic: ceftriaxone
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
ceftriaxone
Generic Name
ceftriaxone
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ceftriaxone sodium 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9858
Product ID
0143-9858_ff2e929e-05bc-4771-9af4-53b52acfd5bc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065342
Listing Expiration
2026-12-31
Marketing Start
2008-01-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439858
Hyphenated Format
0143-9858
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ceftriaxone (source: ndc)
Generic Name
ceftriaxone (source: ndc)
Application Number
ANDA065342 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 25 VIAL in 1 BOX (0143-9858-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9858-01)
Packages (1)
Ingredients (1)
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 (0143-9858-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9858-01)", "package_ndc": "0143-9858-25", "marketing_start_date": "20080110"}], "brand_name": "Ceftriaxone", "product_id": "0143-9858_ff2e929e-05bc-4771-9af4-53b52acfd5bc", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9858", "generic_name": "Ceftriaxone", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA065342", "marketing_category": "ANDA", "marketing_start_date": "20080110", "listing_expiration_date": "20261231"}