ceftriaxone sodium

Generic: ceftriaxone sodium

Labeler: hospira, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ceftriaxone sodium
Generic Name ceftriaxone sodium
Labeler hospira, inc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

ceftriaxone sodium 1 g/1

Manufacturer
Hospira, Inc

Identifiers & Regulatory

Product NDC 0409-7333
Product ID 0409-7333_8e4ee031-a0df-403f-8a7e-de9626a7e501
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065204
Marketing Start 2005-07-20
Marketing End 2027-04-30

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04097333
Hyphenated Format 0409-7333

Supplemental Identifiers

RxCUI
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 sodium (source: ndc)
Generic Name ceftriaxone sodium (source: ndc)
Application Number ANDA065204 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 10 VIAL, SINGLE-USE in 1 CARTON (0409-7333-04) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7333-11)
source: ndc

Packages (1)

0409-7333-04 10 VIAL, SINGLE-USE in 1 CARTON (0409-7333-04) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7333-11)

Ingredients (1)

ceftriaxone sodium (1 g/1)

Linked Drug Pages (2)

Ceftriaxone Sodium ndc-match (0.9) Ceftriaxone Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "8e4ee031-a0df-403f-8a7e-de9626a7e501", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["1665021", "1665046"], "spl_set_id": ["128bb292-d174-4769-b3e6-9f16617f31e3"], "manufacturer_name": ["Hospira, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (0409-7333-04)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7333-11)", "package_ndc": "0409-7333-04", "marketing_end_date": "20270331", "marketing_start_date": "20050720"}], "brand_name": "Ceftriaxone Sodium", "product_id": "0409-7333_8e4ee031-a0df-403f-8a7e-de9626a7e501", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0409-7333", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Hospira, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "1 g/1"}], "application_number": "ANDA065204", "marketing_category": "ANDA", "marketing_end_date": "20270430", "marketing_start_date": "20050720"}