ceftriaxone

Generic: ceftriaxone

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ceftriaxone
Generic Name ceftriaxone
Labeler sagent pharmaceuticals
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

ceftriaxone sodium 1 g/1

Manufacturer
Sagent Pharmaceuticals

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
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021106
Hyphenated Format 25021-106

Supplemental Identifiers

RxCUI
1665005 1665021 1665046
UNII
023Z5BR09K

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (25021-106-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

ceftriaxone sodium (1 g/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"}