ceftriaxone sodium (0781-3206)

Drug Facts

Product Profile

Brand Name ceftriaxone sodium

Generic Name ceftriaxone sodium

Labeler sandoz inc

Dosage Form INJECTION, POWDER, FOR SOLUTION

Routes

INTRAMUSCULAR INTRAVENOUS

Active Ingredients

ceftriaxone sodium 250 mg/1

Manufacturer

Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-3206

Product ID 0781-3206_371d8db2-5d67-4339-92b7-aee2a52b2293

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 07813206

Hyphenated Format 0781-3206

Supplemental Identifiers

RxCUI

309092 1665005 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 ANDA065169 (source: ndc)

Routes

INTRAMUSCULAR INTRAVENOUS

source: ndc

Resolved Composition

Strengths

250 mg/1

source: ndc

Packaging

1 VIAL, SINGLE-USE in 1 CARTON (0781-3206-85) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
10 VIAL, SINGLE-USE in 1 CARTON (0781-3206-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

source: ndc

Packages (2)

0781-3206-85 1 VIAL, SINGLE-USE in 1 CARTON (0781-3206-85) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE 0781-3206-95 10 VIAL, SINGLE-USE in 1 CARTON (0781-3206-95) / 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": "371d8db2-5d67-4339-92b7-aee2a52b2293", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["309092", "1665005", "1665021", "1665046"], "spl_set_id": ["de028434-46cf-44f6-8ac6-889c7c6943b3"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (0781-3206-85)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "0781-3206-85", "marketing_start_date": "20050509"}, {"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (0781-3206-95)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "0781-3206-95", "marketing_start_date": "20050509"}], "brand_name": "Ceftriaxone Sodium", "product_id": "0781-3206_371d8db2-5d67-4339-92b7-aee2a52b2293", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0781-3206", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Sandoz Inc", "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"}