ceftriaxone sodium

Generic: ceftriaxone sodium

Labeler: apotex corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ceftriaxone sodium
Generic Name ceftriaxone sodium
Labeler apotex corp.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

ceftriaxone sodium 10 g/1

Manufacturer
Apotex Corp.

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
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 605056150
Hyphenated Format 60505-6150

Supplemental Identifiers

RxCUI
309090
UPC
0360505615056
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 ANDA209218 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 g/1
source: ndc
Packaging
  • 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (60505-6150-5) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE
source: ndc

Packages (1)

Ingredients (1)

ceftriaxone sodium (10 g/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"}