ceftriaxone
Generic: ceftriaxone
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
ceftriaxone
Generic Name
ceftriaxone
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ceftriaxone sodium 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
25021-106
Product ID
25021-106_71bf5ebd-afe1-4906-86ef-76d7e205ec68
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065329
Listing Expiration
2026-12-31
Marketing Start
2009-11-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021106
Hyphenated Format
25021-106
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
ANDA065329 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 25 VIAL in 1 CARTON (25021-106-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "71bf5ebd-afe1-4906-86ef-76d7e205ec68", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["1665005", "1665021", "1665046"], "spl_set_id": ["5cf93bc5-9e4c-4734-bc02-c7d0ac071022"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-106-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "25021-106-10", "marketing_start_date": "20091105"}], "brand_name": "ceftriaxone", "product_id": "25021-106_71bf5ebd-afe1-4906-86ef-76d7e205ec68", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "25021-106", "generic_name": "ceftriaxone", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ceftriaxone", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "1 g/1"}], "application_number": "ANDA065329", "marketing_category": "ANDA", "marketing_start_date": "20091105", "listing_expiration_date": "20261231"}