ceftriaxone sodium (50090-1875)

Drug Facts

Product Profile

Brand Name ceftriaxone sodium

Generic Name ceftriaxone sodium

Labeler a-s medication solutions

Dosage Form INJECTION, POWDER, FOR SOLUTION

Routes

INTRAMUSCULAR INTRAVENOUS

Active Ingredients

ceftriaxone sodium 250 mg/1

Manufacturer

A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1875

Product ID 50090-1875_48bba686-fc8a-4b5c-97c8-45e926912fd7

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA065169

Listing Expiration 2026-12-31

Marketing Start 2005-05-09

Pharmacologic Class

Classes

cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500901875

Hyphenated Format 50090-1875

Supplemental Identifiers

RxCUI

309092

UNII

023Z5BR09K

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

INTRAMUSCULAR INTRAVENOUS

source: ndc

Resolved Composition

Strengths

250 mg/1

source: ndc

Packaging

10 VIAL, SINGLE-USE in 1 CARTON (50090-1875-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

source: ndc

Packages (1)

50090-1875-0 10 VIAL, SINGLE-USE in 1 CARTON (50090-1875-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

Ingredients (1)

ceftriaxone sodium (250 mg/1)

Linked Drug Pages (1)

Ceftriaxone Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "48bba686-fc8a-4b5c-97c8-45e926912fd7", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["309092"], "spl_set_id": ["1aa0a4ee-1b39-4c3d-a7a3-33dded6fe28c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (50090-1875-0)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "50090-1875-0", "marketing_start_date": "20150616"}], "brand_name": "Ceftriaxone Sodium", "product_id": "50090-1875_48bba686-fc8a-4b5c-97c8-45e926912fd7", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-1875", "generic_name": "Ceftriaxone Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA065169", "marketing_category": "ANDA", "marketing_start_date": "20050509", "listing_expiration_date": "20261231"}