ceftriaxone sodium
Generic: ceftriaxone sodium
Labeler: apotex corp.Drug Facts
Product Profile
Brand Name
ceftriaxone sodium
Generic Name
ceftriaxone sodium
Labeler
apotex corp.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ceftriaxone sodium 10 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
60505-6150
Product ID
60505-6150_7e33cb12-f475-450f-9df3-9158dea19877
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209218
Listing Expiration
2026-12-31
Marketing Start
2019-01-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
605056150
Hyphenated Format
60505-6150
Supplemental Identifiers
RxCUI
UPC
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
ANDA209218 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 g/1
Packaging
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (60505-6150-5) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "7e33cb12-f475-450f-9df3-9158dea19877", "openfda": {"upc": ["0360505615056"], "unii": ["023Z5BR09K"], "rxcui": ["309090"], "spl_set_id": ["ac03a72c-0e35-40f9-b7fc-081badb5f19c"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (60505-6150-5) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE", "package_ndc": "60505-6150-5", "marketing_start_date": "20190121"}], "brand_name": "Ceftriaxone Sodium", "product_id": "60505-6150_7e33cb12-f475-450f-9df3-9158dea19877", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "60505-6150", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "10 g/1"}], "application_number": "ANDA209218", "marketing_category": "ANDA", "marketing_start_date": "20190121", "listing_expiration_date": "20261231"}