ceftriaxone sodium
Generic: ceftriaxone sodium
Labeler: hospira, incDrug Facts
Product Profile
Brand Name
ceftriaxone sodium
Generic Name
ceftriaxone sodium
Labeler
hospira, inc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ceftriaxone sodium 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
0409-7332
Product ID
0409-7332_cc7743b1-4e7b-446a-9ec1-cc234a8bbccf
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065169
Listing Expiration
2027-12-31
Marketing Start
2005-05-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04097332
Hyphenated Format
0409-7332
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 sodium (source: ndc)
Generic Name
ceftriaxone sodium (source: ndc)
Application Number
ANDA065169 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 10 VIAL, SINGLE-USE in 1 CARTON (0409-7332-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7332-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "cc7743b1-4e7b-446a-9ec1-cc234a8bbccf", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["309092", "1665005", "1665021", "1665046"], "spl_set_id": ["03283208-8616-4117-9d2b-aa8046017a4f"], "manufacturer_name": ["Hospira, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (0409-7332-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7332-11)", "package_ndc": "0409-7332-01", "marketing_start_date": "20050509"}], "brand_name": "Ceftriaxone Sodium", "product_id": "0409-7332_cc7743b1-4e7b-446a-9ec1-cc234a8bbccf", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0409-7332", "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": "ANDA065169", "marketing_category": "ANDA", "marketing_start_date": "20050509", "listing_expiration_date": "20271231"}